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. 1,104 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,104 in last 12 months

Showing 15801–15820 of 53,621 recalls

Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Clostridium Difficile GDH Recalled by bioMerieux, Inc. Due to...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Philips Healthcare

Recalled Item: CombiDiagnost R90 is multi-functional general R/F systems. Recalled by...

The Issue: The Aleva monitor requires certain labels to be applied, some of which are...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS FSH Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Philips Healthcare

Recalled Item: ProxiDiagnost N90 is multi-functional general R/F systems. Recalled by...

The Issue: The Aleva monitor requires certain labels to be applied, some of which are...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...

The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Clostridium Difficile Toxin A&B Recalled by bioMerieux, Inc. Due to...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation/RayPlan versions 4 - 11A Recalled by RAYSEARCH LABORATORIES AB...

The Issue: An issue where the combined density in a dose grid voxel partially covered...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS SARS-COV-2 IgM Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Lyme IgG II (LYM) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS PRG Progesterone Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS B.R.A.H.M.S. PROCALCITONIN PCT Recalled by bioMerieux, Inc. Due to...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Philips Healthcare

Recalled Item: DigitalDiagnost C90 Recalled by Philips Healthcare Due to The Aleva monitor...

The Issue: The Aleva monitor requires certain labels to be applied, some of which are...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS SARS-COV-2 IgG Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS DEX@ Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...

The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· MEDTECH SAS

Recalled Item: ROSA One 3.1 Brain application The device is intended for Recalled by...

The Issue: The firm has become aware of a software anomaly affecting ROSA One 3.1 Brain...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Mumps IgG (MPG) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS RUB IgG (RBG) Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
DrugSeptember 22, 2021· New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Recalled Item: Testosterone Cypionate Testosterone Propionate Recalled by New Vitalis...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...

The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

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

Class II — Potential Health HazardOngoing
Refund