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. 1,777 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,777 in last 12 months

Showing 4636146380 of 53,621 recalls

Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: PCP Test (Strip) Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Methadone Test Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: HeartMate II System Controller Product Usage: HeartMate II is a Recalled by...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: HeartMate II LVAD Pump and Pock Controller Kit Recalled by Thoratec...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: Heart Mate II Pocket Controllers removed from packaging Product Usage:...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: HeartMate II Implant Kit with Pocket Controller Recalled by Thoratec...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
FoodMarch 4, 2014· Crown Food Distribution Inc

Recalled Item: Golden Natural Mix Party Net Wt 23.00 oz. in a Recalled by Crown Food...

The Issue: 'Golden Natural' Mix Party contains undeclared sulfites.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Propoxyphene Test Strip Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Amphetamine Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Salmonella typhi Antigen Test Card Recalled by LumiQuick Diagnostics Inc....

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Malaria pf Antigen Test Card Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Malaria pf/pan Antigen Test Card Recalled by LumiQuick Diagnostics Inc. Due...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Tramadol Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Morphine Test Card (2000) Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Syphilis Test Card (Serum) Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: EDDP Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Morphine Strip (300) Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Oxycodone Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: CK-MB Test Card (Whole Blood) Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Syphilis Test Card Whole Blood(Serum) LumiQuick Recalled by LumiQuick...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing