Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,684 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,684 in last 12 months

Showing 2102121040 of 53,621 recalls

FoodJanuary 9, 2020· Wegmans Food Markets, Inc.

Recalled Item: Lobster Stuffed Tilapia 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: Signature Crab Cake 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 Salmon 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: Salmon with Crab Stuffing 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: Lobster Stuffed Mushrooms 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: 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: Crab Stuffed Hot Peppers 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
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 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 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: 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: 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 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: 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: 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