Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,673 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,673 in last 12 months

Showing 2302123040 of 55,896 recalls

DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2019· Alkermes, Inc.

Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...

The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2019· Epic Pharma, LLC

Recalled Item: Estradiol tablets Recalled by Epic Pharma, LLC Due to Presence of Foreign...

The Issue: Presence of Foreign Tablets/Capsules: Estradiol 1 mg was found in a 100...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 26, 2019· AMPLE HILLS MANUFACTURING

Recalled Item: Ample Hills Peppermint Pattie ice cream packed in 3 gallon Recalled by AMPLE...

The Issue: Product may contain undeclared peanut allergen

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 26, 2019· Rong Shing Trading Inc.

Recalled Item: GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard package. 24...

The Issue: Product contains undeclared milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System - Product Usage: Indicated for...

The Issue: Power supply (Model Number: TLC-2003) ME90A2403F01 (24 VDC, 3.75 A, 90 W, 1%...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label and a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 Recalled...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version (IUO) 5.4 Catalog Number: A31774 Recalled...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version 5.6.4 Catalog Number:A33178 OEM Customer...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodSeptember 25, 2019· The Newark Nut Store

Recalled Item: Koppers Chocolate Dark Chocolate Gummy Bears Recalled by The Newark Nut...

The Issue: Kopper s Chocolate has initiated recall of Koppers Chocolate Dark Chocolate...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Rite Aid Pharmacy Maximum Strength Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Equate Maximum Strength Ranitidine Tablets Recalled by Apotex Inc. Due to...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Rite Aid Pharmacy Maximum Strength Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Walgreens Maximum Strength Wal-Zan 150 Ranitidine Tablets Recalled by Apotex...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2019· Apotex Inc.

Recalled Item: Equate Maximum Strength Ranitidine Tablets Recalled by Apotex Inc. Due to...

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund