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. 1,098 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,098 in last 12 months

Showing 21781–21800 of 55,896 recalls

FoodJanuary 9, 2020· Wegmans Food Markets, Inc.

Recalled Item: Lobster Stuffed Haddock Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Products contain undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2020· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Crab Dip with Jalapeno Cheddar Cheese Recalled by Wegmans Food...

The Issue: Products contain undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2020· Wegmans Food Markets, Inc.

Recalled Item: Seafood Lobster Dip Recalled by Wegmans Food Markets, Inc. Due to Undeclared Soy

The Issue: Products contain undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System...

The Issue: The products are being recalled due to reports of breakage broke at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System...

The Issue: The products are being recalled due to reports of breakage broke at the...

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

Class II — Potential Health HazardOngoing
FoodJanuary 9, 2020· Wegmans Food Markets, Inc.

Recalled Item: Crab Pretzel Twist Recalled by Wegmans Food Markets, Inc. Due to Undeclared Soy

The Issue: Products contain undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2020· Wegmans Food Markets, Inc.

Recalled Item: Lobster Stuffed Pretzel Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Products contain undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2020· Wegmans Food Markets, Inc.

Recalled Item: Crab Stuffed Flounder Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Products contain undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware of an issue of incorrect use of the bypass key...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware of an issue of incorrect use of the bypass key...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to A software...

The Issue: A software bug may lead to one image to be assigned to two different...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Uroskop Omnia max Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware of an issue of incorrect use of the bypass key...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A software bug may lead to one image to be assigned to two different...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A software bug may lead to one image to be assigned to two different...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Luminos dRF Max Model: 10762471- Product Usage: is...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Ysio Max - Interventional Fluoroscopic X-Ray System...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage:...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage:...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· CME America, LLC

Recalled Item: CME America BodyGuard Infusion Pump System Recalled by CME America, LLC Due...

The Issue: Infusion Pump Systems may have a delivery inaccuracy of up to 13%, which may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 7, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: cobas infinity core Recalled by Roche Diagnostics Operations, Inc. Due to...

The Issue: Alarm flags that have a "<" symbol in front of them are not displayed on the...

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

Class II — Potential Health HazardOngoing