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. 2,648 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,648 in last 12 months

Showing 3080130820 of 55,896 recalls

Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Large Cheese Filled Cannoli Recalled by Wegmans Food Markets, Inc....

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Marshmellow Treats Tub Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Single Cheese Cannoli Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Cheese Cannoli Tray Recalled by Wegmans Food Markets, Inc. Due to Undeclared Soy

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Marshmellow Treat sold by the pound Recalled by Wegmans Food...

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Dark Bulk Penny Choc Coins Recalled by Wegmans Food Markets, Inc....

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 26, 2017· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Mini Cheese Filled Cannolis 4pk Recalled by Wegmans Food Markets,...

The Issue: Products contain undeclared soy lecithin

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Arterial Access Tray Recalled by Arrow International Inc Due to The povidone...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· ConvaTec, Inc

Recalled Item: SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible...

The Issue: A portion of Lot 7H02242 outer boxes (market units) of the SUR-FIT Natura...

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

Class II — Potential Health HazardOngoing
DrugOctober 25, 2017· Fagron, Inc

Recalled Item: Estriol Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...

The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Dutasteride and Tamsulosin HCl Capsules Recalled by Teva Pharmaceuticals USA...

The Issue: Failed dissolution specifications; all lots within expiry are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 25, 2017· Zimmer Biomet, Inc.

Recalled Item: A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts Recalled...

The Issue: The drill guides were manufactured with the incorrect color anodization.

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

Class II — Potential Health HazardOngoing