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. 2,820 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,820 in last 12 months

Showing 90419060 of 29,496 recalls

Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Bedside PICC CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Neuro Convenience Kit Recalled by Medline Industries Inc Due to NaCl 250 mL...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2021· MAX LUX CORP

Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...

The Issue: Excessive ultraviolet-C radiation

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2021· Smith & Nephew, Inc.

Recalled Item: Smith and Nephew EVOS Self-Tapping Locking Screw SST: (1) Recalled by Smith...

The Issue: The labels on the packages of screws were switched.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2021· Thoratec Corp.

Recalled Item: Abbott HeartMate Touch Communication System Recalled by Thoratec Corp. Due...

The Issue: If LVAS communication system is trying to establish Bluetooth connection and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2021· Atrium Medical Corporation

Recalled Item: The Ocean Water Seal Chest Drain is a plastic Recalled by Atrium Medical...

The Issue: Inadequate/inappropriate Set-Up Instructions, which may result in delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· AMO Manufacturing USA, LLC

Recalled Item: iDesign Recalled by AMO Manufacturing USA, LLC Due to Aberrometer and...

The Issue: Aberrometer and precision laser systems are affected by a remote code...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· AMO Manufacturing USA, LLC

Recalled Item: Catalys Precision Laser System Recalled by AMO Manufacturing USA, LLC Due to...

The Issue: Aberrometer and precision laser systems are affected by a remote code...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of Recalled...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of Recalled...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Biomeme, Inc.

Recalled Item: Biomeme SARS-CoV-2- Real Time RT-PCR Test Recalled by Biomeme, Inc. Due to...

The Issue: The current IFU specifies a shelf-life of one week after resuspension of the...

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

Class II — Potential Health HazardOngoing