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. 2,834 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,834 in last 12 months

Showing 57215740 of 53,621 recalls

FoodJune 7, 2024· Lidl US TRADING

Recalled Item: Chef Select 2 Herb Baguettes Filled With Herb Butter 2x175 Recalled by Lidl...

The Issue: Undeclared wheat and milk (foreign language labeling)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 7, 2024· Randox Laboratories Ltd.

Recalled Item: RX Series CYSC- Cystatin C Reagent -Intended for in vitro Recalled by Randox...

The Issue: Cystatin C Reagent marketed without a 510 (k)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2024· Rygel Advanced Machines d/b/a Omtech Laser

Recalled Item: OMTech Desktop Laser Engraver Recalled by Rygel Advanced Machines d/b/a...

The Issue: Lack of redundant interlocks, missing required labels and certification...

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

Class II — Potential Health HazardOngoing
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE ADVANCED FORMULA Peppermint Recalled by Homeocare Laboratories,...

The Issue: Microbial Contamination of Non-Sterile Products: presence of Terribacillus...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE VEGA Oral Care Recalled by Homeocare Laboratories, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: multiple Bacillus species...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 5, 2024· Beckman Coulter Mishima K.K.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...

The Issue: There are two software bug issues with the analyzer. Issue 1: When a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2024· Philips North America Llc

Recalled Item: SENSE XL TORSO COIL 1.5T. 16-element receive only coil for Recalled by...

The Issue: Potential for coils to heat up and harm patients (burn).

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2024· Philips North America Llc

Recalled Item: SENSE XL TORSO COIL 3.0T. 16-element receive only coil for Recalled by...

The Issue: Potential for coils to heat up and harm patients (burn).

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2024· Philips North America Llc

Recalled Item: SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil Recalled by...

The Issue: Potential for coils to heat up and harm patients (burn).

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

Class I — Serious Health HazardOngoing
DrugJune 4, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Amoxicillin and Clavulanate Potassium Tablets USP Recalled by Teva...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 4, 2024· Beckman Coulter, Inc.

Recalled Item: Dxl 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: The analyzers were built with nonconforming USB cables made with brass...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2024· Zyno Medical LLC

Recalled Item: Zyno Medical Z800 Recalled by Zyno Medical LLC Due to Zyno Medical has found...

The Issue: Zyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: Bag Decanter II Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: Vial Decanter Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: Bottle Decanter Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: C-Flow Bag Decanter Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: Transfer Device Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Qiagen Sciences LLC

Recalled Item: QIAcube Connect MDx - IVD Instrument designed to perform automated Recalled...

The Issue: Heater shaker module does not perform heating if the temperature is set...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: RTL190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: RTLR190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing