FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Hy-Vee Stores Inc
- Product
- Holiday Candy packaged in a 10"/16oz. (UPC 026139100000), 12…
- Reason
- Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
- Published
- March 1, 2017
- Distribution
- Recalle products were distributed only t…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Hy-Vee Stores Inc
- Product
- Peppermint Bark packaged in 4oz. (UPC 026133800000),12 oz. (…
- Reason
- Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
- Published
- March 1, 2017
- Distribution
- Recalle products were distributed only t…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Hy-Vee Stores Inc
- Product
- Dazzled Peanut Brittle packaged in 8oz. (UPC 026267300000) a…
- Reason
- Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
- Published
- March 1, 2017
- Distribution
- Recalle products were distributed only t…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Hy-Vee Stores Inc
- Product
- Cr¿me De Menthe Almond Bark packaged 12 oz. (UPC 02626630000…
- Reason
- Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
- Published
- March 1, 2017
- Distribution
- Recalle products were distributed only t…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Hy-Vee Stores Inc
- Product
- Chocolate almond pretzels packaged in 4 oz. (UPC 02613190000…
- Reason
- Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
- Published
- March 1, 2017
- Distribution
- Recalle products were distributed only t…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Hy-Vee Stores Inc
- Product
- Chocolate almond bark packaged in 4 oz. (UPC 026133400000) a…
- Reason
- Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
- Published
- March 1, 2017
- Distribution
- Recalle products were distributed only t…
View recall →
FDA Recall
Terminated
Historical recordClass II
Mimvey Lo (estradiol and norethindrone acetate tablets USP), 0.5 mg/0.1 mg, 28 tablets per blister card (NDC 0093-5454-18), packaged in 3 blister cards per carton (NDC 0093-5454-62), Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970; Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960.
by Teva Pharmaceuticals USA
- Reason
- Failed Impurities/Degradation Specifications: out of specification test results for the norethindrone impurity.
- Published
- February 22, 2017
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass II
Lisinopril tablets, 5 mg, 1000-count bottle, Rx only, Manufactured for Accord Healthcare, Inc., Durham, NC 27703, NDC 16729-376-17
by ACCORD HEALTHCARE, INC.
- Reason
- Failed tablet/capsule specification: missing break line on the 5mg tablet.
- Published
- February 22, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Taclonex (calcipotriene and betamethasone dipropionate) Topical Suspension, 0.005%/0.064%, packaged in (a) 60 g (NDC 50222-501-06), and (b)120 g (50222-501-66) tubes, Rx Only, Manufactured by: LEO Laboratories Ltd., 285 Cashel Road, Dublin 12 Ireland, Distributed by: LEO Pharma Inc. 1 Sylvan Way, Parsippany, NJ 07054.
by LEO PHARMA INC
- Reason
- Labeling: Incorrect or missing package insert: the affected product was packaged with an out-of-date package insert (PI) dated February 2014.
- Published
- February 22, 2017
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass II
Glipizide extended-release tablets, 2.5mg, 30-count bottle, Rx Only, Manufactured By Patheon Pharmaceuticals Inc Cincinnati OH 45237 USA, NDC 0591-0900-30, UPC 3-0591090030-4
by Actavis Inc
- Reason
- Failed Dissolution Specifications. Above out of specification for dissolution rate observed at the 10 hour testing point.
- Published
- February 22, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only, Manufactured for: Aurobindo Pharma USA, Inc. 2400 Route 130 North, Dayton, NJ 08810 Manufactured by: Aurobindo Pharma Limited Hyderabad-500 072 India, NDC 65862-527-30
by Aurobindo Pharma USA Inc
- Reason
- Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
- Published
- February 22, 2017
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
NOW Foods
- Product
- NOW¿ Multi-Food 1 Tablets, One Tablet Daily, 90 tablets, A D…
- Reason
- Product's supplement fact panel incorrectly states that the product contains 75 mg (milligrams) of Molybdenum, when it actually contains 75 mcg (micrograms).
- Published
- February 22, 2017
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Bwi Inc
- Product
- Burts British Hand Cooked Potato Chips Sea Salt & Malted Vi…
- Reason
- Product is labeled as gluten free; however was labeled as containing an ingredient with gluten.
- Published
- February 22, 2017
- Distribution
- U.S. distribution to the following; MA,…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
The Two Little Guys Company
- Product
- Joe Chips Retro Potato Chips Sour Cream & Toasted Onion Di…
- Reason
- Joe Chips Sour Cream & Toasted Onion Retro Potato Chips contains a seasoning with a milk powder ingredient that may be contaminated with Salmonella although firm testing has not revealed the presence of the bacteria.
- Published
- February 22, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass III
Yum Retaurants International
- Product
- Pizza Hut Creamy Alfredo sauce, case size 40 lbs. 8 bags per…
- Reason
- Foreign object in alfredo sauce. Likely flexible plastic.
- Published
- February 22, 2017
- Distribution
- TX. NC, NY, FL, WI, KY, MI, CA, TN, GA,…
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FDA Recall
Terminated
Historical recordClass III
Aripiprazole Tablets, 2 mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9; Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-3075-3.
by Apotex Inc.
- Reason
- Superpotent Drug: Product may not meet specifications throughout shelf life.
- Published
- February 15, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Pantoprazole Sodium for Injection, 40mg per vial, Single-dose vial, Rx only, Mfd. in India for: Auromedics Pharma LLC 6 Wheeling Road, Dayton, NJ 08810, NDC 55150-202-00
by Aurobindo Pharma USA Inc
- Reason
- Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance.
- Published
- February 15, 2017
- Distribution
- Nationwide
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FDA Recall
Terminated
Historical recordClass II
Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50 unit dose cups per case (NDC 66689-047-50), Rx only, Xact Dose, Manufactured by VistaPharm, Largo, FL 33771.
by VistaPharm, Inc.
- Reason
- Defective Container: Leakage of unit dose cups that may occur at the seal.
- Published
- February 15, 2017
- Distribution
- Domestic: AL, AZ, CA, CO, CT, FL, GA, HI…
View recall →
FDA Recall
Terminated
Historical recordClass III
Olanzapine tablets, USP, 2.5 mg, packaged in a 30-count bottle, Rx only, Mfd: By: Dr. Reddy's Laboratories Limited, Bachupally, India, NDC 55111-163-30
by Dr. Reddy's Laboratories, Inc.
- Reason
- Failed impurities/degradation specifications: due to out-of-specification result for the Related Substance Compound C (Impurity 6 - N-Oxide at the 18 month stability station.
- Published
- February 15, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Circle U Foods, Inc
- Product
- Circle U Foods, Inc. Product Code: 211013 NPP/Elmer's Deli S…
- Reason
- Potential glass inclusion
- Published
- February 15, 2017
- Distribution
- Multiple states
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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