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. 1,139 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,139 in last 12 months

Showing 9001–9020 of 29,496 recalls

Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 3, 2021· Haag-Streit USA Inc

Recalled Item: OCT-Camera 211 01 A3 Recalled by Haag-Streit USA Inc Due to Malfunction of...

The Issue: Malfunction of the automatic laser beam shut-off, the OCT unit might not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2021· Leica Microsystems, Inc.

Recalled Item: Leica Microsystems M220 F12 Microscope Systems Recalled by Leica...

The Issue: In May 2021, Leica Microsystems received one (1) complaint pertaining to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2021· Haag-Streit USA Inc

Recalled Item: OCT-Camera 211 01 A1 Recalled by Haag-Streit USA Inc Due to Malfunction of...

The Issue: Malfunction of the automatic laser beam shut-off, the OCT unit might not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II DUODENOVIDEOSCOPE OLYMPUS TJF-Q180V Model Number: TJF-Q180V...

The Issue: Use of a TJF-Q180V with adhesive deterioration or other damages may pose a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: RoyalSilk Non-Reinforced Surgical Gowns X-large SKU: 9548 Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: RoyalSilk Non-Reinforced Surgical Gowns Large SKU: 9518 Recalled by Cardinal...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Magnolia Medical Technologies, Inc.

Recalled Item: The Steripath Gen2 Blood Collection System Model Number/Description...

The Issue: Due to an uptick of complaints associated with premature needle retraction...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Flower Orthopedics Corporation

Recalled Item: Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be...

The Issue: Mating incompatibility between the Inserter Shaft and the Inserter Draw Rod...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: RoyalSilk Non-Reinforced Surgical Gowns XXX-large Recalled by Cardinal...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040 Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: SmartGown Breathable Surgical Gowns with raglan sleeves X-large Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns XX-large SKU: 9070 Recalled...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing