Food recalls in the United States in 2013 · page 21
2,111 official food recall notices published by the U.S. Food and Drug Administration (FDA) in the United States in 2013, newest first. Each notice links to the official page.
Notices
2,111 notices, newest first · page 21 of 43.
- October 30, 2013reportedFDAClass IUndeclared allergen
NatureMost LABORATORIES NATURAL WHEY POWER W / YERBA MATE VANILLA / ALMOND Dietary Supplement NET WEIGHT 3 LBS. (1362g). Product Number: 9950
Official wording (English):
Undeclared allergens, milk,almond and soy.
- October 30, 2013reportedFDAClass IUndeclared allergen
NatureMost LABORATORIES NATURAL WHEY POWER W / YERBA MATE STRAWBERRY / BANANA Dietary Supplement NET WEIGHT 3 LBS. (1362g).
Official wording (English):
Undeclared allergens, milk and soy.
- October 30, 2013reportedFDAClass IListeria
Green Leaf Lettuce is sold in bulk cases under "Garre Farms" or "Rossi Farms" brand. There are 24 heads of green leaf lettuce packed in each cardboard box. The…
Official wording (English):
Garre Farms is recalling green leaf lettuce due to a potential contamination with Listeria monocytogenes.
- October 30, 2013reportedFDAClass IOther reason
Frozen Sliced Carrots, packaged in 2 lbs. bag, sold under Simplot Classic brand. The UPC is 0 71179 1846 3 1. The product is labeled in parts: "***SIMPLOT…
Official wording (English):
Green shelled soybeans (Edamame) are potentially mixed in with sliced carrots.
- October 23, 2013reportedFDAClass IUndeclared allergen
Hartley's Potato Chips Salt & Vinegar 4.5 oz and 2.5 oz bags Hartley's Potato Chip Co., Inc, Lewistown, PA Ingredients: potatoes, vegetable shortening, salt…
Official wording (English):
Undeclared lactose (milk) in seasoning sub-ingredient used in the manufacturing of Hartley's Salt & Vinegar Potato Chips.
- October 23, 2013reportedFDAClass IUndeclared allergen
Wegmans Bakery Mini Muffins APPLE CINNAMON, NET WT 14 OZ (397g) , UPC 77890 18951 --- Baked By Wegmans Food Markets Inc., Rochester, NY 14603
Official wording (English):
The Apple Cinnamon Mini Muffins contain undeclared soy, a known allergen.
- October 23, 2013reportedFDAClass IIUndeclared allergen
Talenti German Chocolate Cake Gelato, One Pint (473 mL), Crafted By: Talenti, Marietta, GA 30062.
Official wording (English):
Product contains undeclared Allergen; Almonds.
- October 23, 2013reportedFDAClass IIUndeclared allergen
Honey Roasted Peanuts, net wt. 11 oz.., packed in a clear plastic bag. Ingredients: peanuts, sugar, peanut and/or canola and/or cottonseed oil, honey, salt…
Official wording (English):
Honey Roasted Peanuts were recalled due to undeclared milk (lactose) and wheat (wheat starch) allergens in the ingredient statement.
- October 23, 2013reportedFDAClass IIUndeclared allergen
Roasted Salted Mixed Nuts w/ Peanuts, net wt. 12 oz., packed in a clear plastic bag. Ingredients: blanched peanuts, unblanched peanuts, unblanched almonds…
Official wording (English):
Roasted Salted Mixed Nuts with Peanuts were recalled for undeclared tree nuts (pecans) in the ingredient statement.
- October 9, 2013reportedFDAClass IIOther reason
Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, packaged in 5.7-oz. (35 servings) bottles, UPC 300670068356, 9.4-oz (58…
Official wording (English):
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
- October 9, 2013reportedFDAClass IIOther reason
Benefiber Plus Heart Health Non-Thickening Powder, Sugar Free, packaged in 6.4-oz (48 servings) bottles, UPC 300673002487. Distributed by: Novartis Consumer…
Official wording (English):
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
- October 9, 2013reportedFDAClass IIOther reason
Benefiber Fiber Drink Mix, Cherry Pomegranate, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670107246. Distributed by…
Official wording (English):
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
- October 9, 2013reportedFDAClass IIOther reason
Benefiber Fiber Drink Mix, Kiwi Strawberry, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670106249. Distributed by…
Official wording (English):
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
- October 9, 2013reportedFDAClass IIOther reason
Benefiber Fiber Supplement Plus Calcium, Orange Natural Flavor, Sugar Free, packaged in 10.76-oz (48 Servings) bottles, UPC 300670108489. Distributed by…
Official wording (English):
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
- October 9, 2013reportedFDAClass IIOther reason
Benefiber Non-Thickening Powder, Sugar Free, packaged in the following configurations: (1) 2.8-oz. (20 servings) bottles, UPC 300670044206; (2) 4.6-oz. (32…
Official wording (English):
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
- October 9, 2013reportedFDAClass IIIOther reason
Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028
Official wording (English):
Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.
- October 9, 2013reportedFDAClass IIIOther reason
Tully's House Blend Decaffeinated K-Cup¿ Packs (12-ct retail box) Product Code: 8803; UPC: 099555088038
Official wording (English):
Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.
- October 2, 2013reportedFDAClass IUndeclared allergen
First Street Blueberry Muffins (S 45395), 14 oz., 9 trays/case, UPC 0 4151210833 4
Official wording (English):
Bubbles Baking Co. is recalling Blueberry muffins and Loaf cakes because they may contain undeclared milk and soy.
- October 2, 2013reportedFDAClass IUndeclared allergen
First Street Blueberry Muffins Loaf (S 45383), 16 oz., 12 trays/case, UPC 0 41512 10854 9.
Official wording (English):
Bubbles Baking Co. is recalling Blueberry muffins and Loaf cakes because they may contain undeclared milk and soy.
- October 2, 2013reportedFDAClass IListeria
spartan fresh selections american potato salad, Net Wt. 16 oz (1 LB) 454g. UPC 11213-90320.
Official wording (English):
One lot of Spartan Fresh Selections American Potato Salad has the potential to be contaminated with Listeria monocytogenes.
- October 2, 2013reportedFDAClass IIForeign body
Meijer 8 Inch Carrot Uniced Split Cake Layers (product is packed in bulk cartons of 24 units/paper bags lined with flexible blue plastic liner).
Official wording (English):
Product was found to contain foreign material, flexible plastic.
- October 2, 2013reportedFDAClass IIUndeclared allergen
Breaded, frozen shrimp packaged in plastic bags labeled in part: BREADED SHRIMP; NET WEIGHT; 2.0 LBS or 3 LBS
Official wording (English):
Packages of breaded shrimp failed to declare shellfish (shrimp) and wheat allergens.
- October 2, 2013reportedFDAClass IIIChemical contaminant or residue
Fresh Herbs Everyday Basil, Shenandoah Growers brand, packaged in .75 oz; 2 oz.; and 2.5 oz. in 3 count and 6 count cardboard sleeves and labeled in part…
Official wording (English):
Fresh basil may be adulterated with pesticides.
- October 2, 2013reportedFDAClass IIIChemical contaminant or residue
Basil, fresh, Giant brand, packaged in 2.5 oz. package and labeled in part ***Distributed by FoodHold USA Landover, MD 20785***
Official wording (English):
Fresh basil may be adulterated with pesticides.
- October 2, 2013reportedFDAClass IIILabelling error
Dietary Supplements under the same formulation, Labeled and Packaged in the Following: MAX Brand Proste-Support, 150 Count Tablets. Product labeling reads in…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand Glucosamine 1500 mg + MSM 400 mg, 120 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400 mg…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand Glucosamine 1500 mg + MSM 400 mg, 300 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400 mg…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand Glucosamine 1500 mg, Plus MSM + Vit D 200 Count Tablets Product labeling reads in part:"MAX Glucosamine 1500mg***200 Tablets***6 65176 60566…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
Dietary Supplement labeled and packaged under the following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX Brand LIVER STRONG 200 Count…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX LIVERAID Dietary Supplement 200 Counts***6 65176 35168 6***Manufactured in FDA…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass ILabelling error
MAX Brand SUPER SELENIUM 250, 180 Count Tablets Product labeling reads in part:"MAX SUPER SELENIUM 250 ***Dietary Supplement 180 Tablet***0 65176 06756…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand BRAZILIAN BEE PROPOLIS, 180 Count Softgels Product labeling reads in part:"MAX***BRAZILIAN BEE PROPOLIS DIETARY SUPPLEMENT 180 Softgels***6 65176…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IILabelling error
MAX Brand Bio-Cell Collagen II, 100 Count Softgels Product labeling reads in part:"MAX Bio-Cell CollagenII Dietary Supplement 100 Softgels*** 0 65176 08108…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IILabelling error
Hyper II DHA/EPA, 100 Count Softgels. Product labeling reads in part:"Hyper II DHA/EPA Refined Deep Sea Fish Oil 50% DHA - 30% EPA***Dietary Supplement 100…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:"Hyper II LECITHIN***Dietary Supplement 100 Softgels***6 65176 01115 3***Manufactured…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX Brand…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:"MAX Stem Cell Enhance***1.0fl. oz(30ml)***".
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand CoQ10, 90 Count Capsules Product labeling reads in part:"MAX CoQ10***DIETARY SUPPLEMENT 90 Capsules***6 65176 30162 9***Manufactured in FDA Approved…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX GOUT AID***Dietary Supplement 130 Tablets***6 0 65176 26512 7***HealthMax Products…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX LIVER STRONG, 200 Count Capsules Product labeling reads in part:"MAX LIVER STRONG CoQ10***Dietary Supplement 200 Capsules***6 65176 32608 0***Manufactured…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG AID, 100 Count Capsules; MAX Brand POMEGRANATE, 100 Count…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads in part:"MAX Nitric Oxide Enhance***DIETARY SUPPLEMENT 90 Capsules***0 65176 55958…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand Organic Blueberry, 100 Count Capsules Product labeling reads in part:"MAX Organic Blueberry***Dietary Supplement 100 CAPSULES***6 65176 62165…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand Organic OPC31 Grapeseed Extract, 200 Count Capsules. Product labeling reads in part:"MAX Organic OPC31 Grapeseed Extract***NEW WITH…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part:"MAX ORGANIC OPC69 MAXIMUM STRENGTH***DIETARY SUPPLEMENT 300 Capsules***0 65176…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:"MAX RESVERATROL***Dietary Supplement 120 CAPSULES***Manufactured in FDA Approved…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: MAX Brand SOY ISOFLAVONES, 90 Count Capsules; MAX Brand ULTRA…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
MAX Brand CoQ-10, 780mg, 300 Count Capsules. Product labeling reads in part:"MAX CoQ-10 80 mg***DIETARY SUPPLEMENT 300 Capsules***6 65176 25166…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
Max Blood Sugar Defense 150 tablets Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT 150 tablets***Manufactured for:HealthMax Products…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
- October 2, 2013reportedFDAClass IIILabelling error
Max LUNG AID Extra Strength 100 capsules Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT 100 capsules***Manufactured for:HealthMax…
Official wording (English):
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
Sources: openFDA (U.S. FDA food enforcement reports), CC0 · Health Canada / CFIA Recalls and Safety Alerts, Open Government Licence – Canada · Food Standards Agency food alerts, OGL v3 · RappelConso (DGCCRF), Licence Ouverte 2.0. Shares and counts: Shelfpedia calculations.