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. 2,868 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,868 in last 12 months

Showing 45814600 of 55,896 recalls

FoodOctober 3, 2024· Youngstown Grape Distributors, Inc.

Recalled Item: Farmers Juice Focus Greens packaged in a 12 fl. oz. bottle Recalled by...

The Issue: Incomplete pasteurization

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 3, 2024· Youngstown Grape Distributors, Inc.

Recalled Item: Farmers Juice Watermelon Hydration packaged in a 12 fl. oz. bottle Recalled...

The Issue: Incomplete pasteurization

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal CHILDREN'S LAPTRACEPACK Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal CHILDREN'S ORTHOPEDIC TRACEPACK Recalled by DeRoyal Industries Inc...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal CHILDREN'S GENERAL TRACEPACK Recalled by DeRoyal Industries Inc Due...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· GE Healthcare

Recalled Item: GE Healthcare Centricity Universal Viewer Zero Footprint Recalled by GE...

The Issue: GE HealthCare has become aware of an issue in Centricity Universal Viewer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· DeRoyal Industries Inc

Recalled Item: DeRoyal C-SECTION TRACEPACK Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Medtronic Perfusion Systems

Recalled Item: Medtronic DLP Aortic Root Cannula with Flow-Guard Recalled by Medtronic...

The Issue: There is the potential for a potential sterility breach for three lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2024· Smith & Nephew Medical, Ltd.

Recalled Item: RENASYS EDGE The RENASYS¿ EDGE pump is indicated for patients Recalled by...

The Issue: Due to issues with battery depletion and inability to recharge if the...

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

Class II — Potential Health HazardOngoing
DrugOctober 1, 2024· ACCORD HEALTHCARE, INC.

Recalled Item: Cisplatin Injection Recalled by ACCORD HEALTHCARE, INC. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 1, 2024· Advanced Medical Solutions Ltd.

Recalled Item: MEDLINE MAXORB EXTRA ALGINATE WOUND DRESSING 4X4 SQUARE Recalled by Advanced...

The Issue: Due to defects on primary packaging pouch that compromise the device's...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2024· Advanced Medical Solutions Ltd.

Recalled Item: Hollister CalciCare Calcium Alginate Dressing calcium alginate dressings...

The Issue: Due to defects on primary packaging pouch that compromise the device's...

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

Class II — Potential Health HazardOngoing