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. 2,901 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,901 in last 12 months

Showing 13411360 of 55,896 recalls

Medical DeviceSeptember 19, 2025· Kico Knee Innovation Company

Recalled Item: Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number:...

The Issue: Complaint identified issue with AI surgical planning software that may...

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

Class II — Potential Health HazardOngoing
FoodSeptember 18, 2025· Goyal Group Inc.

Recalled Item: 1. SILVER HORSE - PURE ALUMINIUM MADE IN INDIA - Recalled by Goyal Group...

The Issue: Contains elevated levels of lead

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2025· Egress Capital Partners Inc.

Recalled Item: Taproom Gourmet brand 20lb and 18lb bulk "Fifth Avenue" Mix Recalled by...

The Issue: No ingredient label. Product contains undeclared allergens (peanuts,...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2025· Egress Capital Partners Inc.

Recalled Item: Taproom Gourmet brand 15lb bulk "Madison" Mix Recalled by Egress Capital...

The Issue: No ingredient label. Product contains undeclared allergens (peanuts,...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2025· Egress Capital Partners Inc.

Recalled Item: Taproom Gourmet brand 15lb bulk "Broadway" Mix Recalled by Egress Capital...

The Issue: No ingredient label. Product contains undeclared allergens (peanuts, sesame,...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2025· Egress Capital Partners Inc.

Recalled Item: Taproom Gourmet brand 20lb bulk "Park" Mix Recalled by Egress Capital...

The Issue: No ingredient label. Product contains undeclared allergens (peanuts,...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2025· Egress Capital Partners Inc.

Recalled Item: Taproom Gourmet brand 18lb bulk "Empire" Mix Recalled by Egress Capital...

The Issue: No ingredient label. Product contains undeclared allergens (cashews,...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2025· Western United Fish Company Inc

Recalled Item: Kirkland Signature brand Ahi Tuna Wasabi Poke Recalled by Western United...

The Issue: Listeria monocytogenes. Recall was initiated after being notified by green...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Recalled...

The Issue: Software issue for hq analyzer results in system not visibly applying...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Recalled...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump"...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Recalled...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· HeartSine Technologies Ltd

Recalled Item: HeartSine Pad-Pak Recalled by HeartSine Technologies Ltd Due to Due to...

The Issue: Due to customer complaints, defibrillator pads may contain damage pins that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cardinal Health 200, LLC

Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Recalled...

The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· GE Medical Systems, LLC

Recalled Item: LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7....

The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· GE Medical Systems, LLC

Recalled Item: LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7....

The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· Cook Medical Incorporated

Recalled Item: Zenith Alpha 2 Thoracic Endovascular Graft Recalled by Cook Medical...

The Issue: Affected devices may contain PTFE coating scrapings. Scrapings could be...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2025· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Airvo 2 Recalled by Fisher & Paykel Healthcare, Ltd. Due to When...

The Issue: When unintentionally disconnected from power source, humidifier device (used...

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

Class II — Potential Health HazardOngoing