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. 2,642 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,642 in last 12 months

Showing 2870128720 of 29,496 recalls

Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair. The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· KCI USA, Inc.

Recalled Item: RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention...

The Issue: The firm is initiating a voluntary medical device correction for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Mar Cor Purification

Recalled Item: Mar Cor Purification CWP Reverse Osmosis System. Models 101 Recalled by Mar...

The Issue: There exists a potential situation with the crimp connection at the pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential issue due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Bridgepoint Medical

Recalled Item: BridgePoint Medical Recalled by Bridgepoint Medical Due to BridgePoint...

The Issue: BridgePoint Medical Inc. is voluntarily recalling Stingray Catheter, Model...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece...

The Issue: Disposable T-Piece circuits used with resuscitation systems are unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 26, 2012· Sunrise Medical (US) LLC

Recalled Item: Padded Swing Away Arm Rest with Receiver Recalled by Sunrise Medical (US)...

The Issue: Reports of injury when the Padded Swing Away Armrest is used for full body...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***Press FT***2.6 w/ One #2 (5 metric) Hi-Fi***Suture Recalled by Linvatec...

The Issue: Linvatec Corporation DBA ConMed Linvatec in Largo, FL is recalling Press FT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: NP211H***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO Recalled by...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***PressFT***2.1 w/ One #2 (5 metric)...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***PressFT***2.6 w/ Two #1 (4 metric)...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***PressFT***2.1 w/ Two #0 (3.5 metric)...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***PressFT***2.6 w/ One #2 (5 metric)...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V. The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Electronic O2 Blender/Analyzer. The...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing