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. 2,889 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,889 in last 12 months

Showing 33813400 of 55,896 recalls

Medical DeviceFebruary 10, 2025· Immuno-Mycologics, Inc

Recalled Item: Candida ID Antigen Recalled by Immuno-Mycologics, Inc Due to Candida...

The Issue: Candida Immunodiffusion Antigen may have reduced sensitivity which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2025· Brainlab AG

Recalled Item: Origin Data Management software versions 3.1.0 Recalled by Brainlab AG Due...

The Issue: Under certain circumstances, it can occur that patient records from...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2025· Alcon Research LLC

Recalled Item: Alcon Custom Pak with Non-Latex Symbol Recalled by Alcon Research LLC Due to...

The Issue: Customer-designed sterile surgical procedure packs contain latex components...

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

Class II — Potential Health HazardOngoing
FoodFebruary 7, 2025· Rong Shing Trading NY Inc

Recalled Item: LEMON PLUM Recalled by Rong Shing Trading NY Inc Due to Product contains...

The Issue: Product contains cyclamates.

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 7, 2025· CardioFocus, Inc.

Recalled Item: CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial...

The Issue: Damage to the sterile barrier pouch of catheter, which could potentially...

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

Class II — Potential Health HazardOngoing
DrugFebruary 6, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Morphine Sulfate Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2025· Padagis US LLC

Recalled Item: Estradiol Gel Recalled by Padagis US LLC Due to Defective Container: Some...

The Issue: Defective Container: Some packets may not be fully sealed, potentially...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DR DIULUS INJECTION PACK Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LABOR & DELIVERY PPS Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters...

The Issue: Devices may have higher than expected amounts of bacterial endotoxin.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: MAJOR VASCULAR PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LABOR & DELIVERY PACK Recalled by American Contract Systems Inc Due to ACS...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: CENTRAL LINE PICC Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DIAGNOSTIC NEURO IR TRAY Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: GENERAL LAPAROSCOPIC PACK-LF Recalled by American Contract Systems Inc Due...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: C-SECTION PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DELIVERY PACK Recalled by American Contract Systems Inc Due to ACS is unable...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: OPEN HEART ADULT - SIDE A Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: HIP SCOPE Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LACERATION TRAY Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing