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. 2,678 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,678 in last 12 months

Showing 2136121380 of 55,896 recalls

FoodFebruary 24, 2020· Tova Industries Inc

Recalled Item: National Food Group brand Soup Base Vegetable Recalled by Tova Industries...

The Issue: Downstream recall from supplier. Possible metal shavings in ingredient.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2020· Sierra Soups

Recalled Item: Sierra Soups Pasta e Fagioli: All Natural Vegetarian Vegan (without pasta)...

The Issue: Firm was notified that their Gluten Free Soup mix labeling is misleading as...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2020· Breckenridge Pharmaceutical, Inc

Recalled Item: Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL) Recalled by Breckenridge...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 21, 2020· Akorn, Inc.

Recalled Item: CVS Health Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn, Inc....

The Issue: Presence of Particulate Matter: Brown spots observed on the inside of the...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 21, 2020· Akorn, Inc.

Recalled Item: Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn, Inc. Due to...

The Issue: Presence of Particulate Matter: Brown spots observed on the inside of the...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 21, 2020· Akorn, Inc.

Recalled Item: Well at Walgreens Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn,...

The Issue: Presence of Particulate Matter: Brown spots observed on the inside of the...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 21, 2020· Moonstruck Chocolate Company

Recalled Item: Moonstruck Praline Pecan & Ginger Element Bar in Dark Chocolate Recalled by...

The Issue: Undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 21, 2020· Kaiser Pickles LLC

Recalled Item: Kaiser Mild Banana Pepper Rings 1/4 KK in 1 gallon Recalled by Kaiser...

The Issue: Possible foreign material.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 21, 2020· Epimed International

Recalled Item: R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496...

The Issue: Incorrect expiration date on introduction cannula packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Epimed International

Recalled Item: R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124...

The Issue: Incorrect expiration date on introduction cannula packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Qiagen Sciences LLC

Recalled Item: AmniSure ROM Test Recalled by Qiagen Sciences LLC Due to An image on the...

The Issue: An image on the associated polybag contains an incorrect rinse time of 30...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2020· Radiometer Medical ApS

Recalled Item: TCM4 Base unit Recalled by Radiometer Medical ApS Due to Reports have been...

The Issue: Reports have been received about the transcutaneous monitoring system...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Avalon Elite Vascular Access Kit Recalled by Maquet Cardiovascular Us Sales,...

The Issue: A lot of Avalon Elite Vascular Access Kits (VAK) are being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2020· Philips North America, LLC

Recalled Item: Expression MR400 MRI Patient Monitoring System Model Number: 866185 Software...

The Issue: Menu selections for users to access the oxygen (O2) sensor calibration were...

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

Class II — Potential Health HazardOngoing
DrugFebruary 20, 2020· Teva Pharmaceuticals USA

Recalled Item: Mesalamine Delayed-Release Tablets Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Dissolution Specifications: Low out of specification dissolution...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2020· Haemonetics Corporation

Recalled Item: TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0...

The Issue: Software defect in TEG Manager impacts the displayed alert for out of range...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing