FDA Recall
TerminatedTerminated: April 20, 2020Historical recordClass II
Choice Antibacterial Hand Soap, (ethyl alcohol 61%) 800 ml/ 27 fl oz, Universal Valve, Inopak LTD, Ringwood, NJ
by Inopak Ltd
- Reason
- GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump.
- Published
- October 11, 2017
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: April 20, 2020Historical recordClass II
Mild Healthcare Antibacterial Hand Soap, 6% P.C.M.X., 1000 mL and 2000 mL Disc Pump, 800 mL Universal Valve, and 1 gallon bottles, Inopak. Ltd, Ringwood, NJ 07456
by Inopak Ltd
- Reason
- GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump.
- Published
- October 11, 2017
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: April 20, 2020Historical recordClass II
Option Systems Antibacterial Foaming Hand Wash, 0.3% P.C.M.X., 8 fl oz and 18 fl oz. bottles and 500, mL 800 mL, and 1000 mL pouches, ALSO labeled as STYLE Antibacterial Hand Soap, Inopak Ltd Ringwood, NJ --- NDC 5031-431-02
by Inopak Ltd
- Reason
- GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump
- Published
- October 11, 2017
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: July 16, 2020Historical recordClass III
Deferoxamine Mesylate for injection, USP, Single-use Vial, 500 mg/vial, 10 mL vial. Intravenous, Intramuscular, Subcutaneous Use, Rx Only, Hospira, Inc., Lake Forest IL USA, NDC 0406-2336-10.
by Pfizer Inc.
- Reason
- CGMP Deviations: Firm failed to control impurity for color change at the API stage.
- Published
- October 11, 2017
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: June 11, 2020Historical recordClass I
Cargill Cocoa and Chocolate, Inc.
- Product
- Shoprite Real Semi-Sweet Chocolate Chips, Net Wt. 24 oz., UP…
- Reason
- Cargill Cocoa & Chocolate is recalling Shoprite Real Semi-Sweet Chocolate Chips due to undeclared milk.
- Published
- October 11, 2017
- Distribution
- Shop Rite and The Fresh Grocer and other…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: September 17, 2021Historical recordClass I
Garden Of Life, LLC
- Product
- Garden of Life, Baby Organic Liquid probiotic formula, 56 ml…
- Reason
- The product may pose a choking hazard to newborns due to the thickness of the liquid.
- Published
- October 11, 2017
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: October 13, 2020Historical recordClass II
Grand Supercenter Inc.
- Product
- HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G),…
- Reason
- The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen.
- Published
- October 11, 2017
- Distribution
- Products are mostly distributed to store…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: October 13, 2020Historical recordClass II
Grand Supercenter Inc.
- Product
- HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G),…
- Reason
- The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen.
- Published
- October 11, 2017
- Distribution
- Products are mostly distributed to store…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: October 13, 2020Historical recordClass II
Grand Supercenter Inc.
- Product
- HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G),…
- Reason
- The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen.
- Published
- October 11, 2017
- Distribution
- Products are mostly distributed to store…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: October 13, 2020Historical recordClass II
Grand Supercenter Inc.
- Product
- HAIOREUM, RICE POP SNACK, KOREAN STYLE SNACK 0.41 LBS (190 G…
- Reason
- The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen.
- Published
- October 11, 2017
- Distribution
- Products are mostly distributed to store…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: December 12, 2017Historical recordClass II
Pro Bioteks Laboratories
- Product
- Bio35, Vitamin-Mineral Omega Oils Trace Minerals Dietary Sup…
- Reason
- Bio-35 has undeclared soy lecithin.
- Published
- October 11, 2017
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 8, 2019Historical recordClass II
KIND LLC
- Product
- KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.…
- Reason
- Outer box fails to declare the allergen walnuts, the individual bar is properly labeled
- Published
- October 11, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: April 8, 2019Historical recordClass III
Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs (NDC 0781-3407-95), Rx only, Manufactured in Austria by Sandoz GmbH or Sandoz Inc., Princeton, NJ 08540.
by Sandoz Inc
- Reason
- Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
- Published
- October 4, 2017
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: June 21, 2018Historical recordClass II
Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; NDC 16252-523-01.
by Teva Pharmaceuticals USA
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: An incorrect expiration date of July 2018 is printed on the product labeling rather than the correct expiration date of July 2017.
- Published
- October 4, 2017
- Distribution
- Nationwide
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FDA Recall
TerminatedTerminated: January 24, 2020Historical recordClass II
Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24
by Pfizer Inc.
- Reason
- Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.
- Published
- October 4, 2017
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: February 22, 2018Historical recordClass I
House Of Thaller Inc
- Product
- Marketside CLASSIC HUMMUS WITH PINE NUTS NET WT. 10 oz (283g…
- Reason
- The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
- Published
- October 4, 2017
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 22, 2018Historical recordClass I
House Of Thaller Inc
- Product
- LANTANA White Bean HUMMUS NET WT. 10 oz (283g)
- Reason
- The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
- Published
- October 4, 2017
- Distribution
- Product was shipped to the following sta…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 22, 2018Historical recordClass I
House Of Thaller Inc
- Product
- FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283…
- Reason
- The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.
- Published
- October 4, 2017
- Distribution
- Product was shipped to the following sta…
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FDA Recall
TerminatedTerminated: January 11, 2019Historical recordClass I
Activase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 single-dose 100ml vial of sterile water for Injection USP and one transfer device. Manufactured by: Genentech, Inc. 1 DNA Way, South San Francisco, CA 84080-4990. NDC: 50242-0085-27
by Genentech, Inc.
- Reason
- Non-Sterility:presence of cracked or chipped glass at the neck of Sterile Water for Injection vials.
- Published
- September 27, 2017
- Distribution
- Nationwide
View recall →
FDA Recall
TerminatedTerminated: December 4, 2018Historical recordClass II
Aminocaproic Acid, USP (6-Aminohexanoic Acid) active pharmaceutical ingredient, packaged in a) 100 g jar (NDC 38779-0989-05, b) 1 kg jar (NDC 38779-0989-09), and 25 kg drum (NDC 38779-0989-07), Rx only, Packed by Medisca Inc., Plattsburgh, NY 12901, CAS: 60-32-1. 38779-0989-05; jar, 300 ml, white HDPE 38779-0989-07; drum, 15 gallon, Fiber 38779-0989-09; 2.8L, white, HDPE
by Medisca, Inc.
- Reason
- CGMP Deviations: Product manufactured for Industrial Use but was labeled and distributed for Pharmacy Compounding Use.
- Published
- September 27, 2017
- Distribution
- Nationwide
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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