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. 1,110 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,110 in last 12 months

Showing 13941–13960 of 53,621 recalls

Medical DeviceMarch 30, 2022· Abbott Vascular

Recalled Item: Dragonfly OpStar Imaging Catheter Recalled by Abbott Vascular Due to There...

The Issue: There is a potential that the proximal marker may separate from the imaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2022· Accriva Diagnostics, Inc.

Recalled Item: The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 Recalled by...

The Issue: Two whole blood Platelet Reactivity tests exist that share the same reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Medtronic Neuromodulation

Recalled Item: Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200...

The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2022· Devicor Medical Products Inc

Recalled Item: HydroMARK Breast Biopsy Marker Recalled by Devicor Medical Products Inc Due...

The Issue: Small patient labels do not match the primary device label. The primary...

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

Class II — Potential Health HazardOngoing
DrugMarch 30, 2022· Unilever United States Inc.

Recalled Item: Suave 24-Hour Protection Aerosol Antiperspirant Fresh scent Recalled by...

The Issue: CGMP Deviation; manufactured at the same facility where other lots were...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2022· Unilever United States Inc.

Recalled Item: Suave 24-Hour Protection Aerosol Antiperspirant Powder scent Recalled by...

The Issue: Chemical contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 30, 2022· Skippy Foods, LLC.

Recalled Item: SKIPPY Creamy Peanut Butter Blended with Plant Protein NET WT Recalled by...

The Issue: Potential to contain small steel contaminants.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 30, 2022· Skippy Foods, LLC.

Recalled Item: SKIPPY Reduced Fat Chunky Peanut Butter NET WT 16.3 oz Recalled by Skippy...

The Issue: Potential to contain small steel contaminants.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 30, 2022· Skippy Foods, LLC.

Recalled Item: SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz Recalled by Skippy...

The Issue: Potential to contain small steel contaminants.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 29, 2022· Philips North America Llc

Recalled Item: The device is a whole-body CT x-ray system. The acquired Recalled by Philips...

The Issue: Three software issues affecting incorrect image display, error interpreting...

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

Class II — Potential Health HazardOngoing
DrugMarch 29, 2022· Pink Toyz

Recalled Item: Pink Pussycat SENSUAL ENHANCEMENT capsule Recalled by Pink Toyz Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 29, 2022· Best Brands Consumer Products, Inc.

Recalled Item: Mickey Mouse Hand Sanitizer Recalled by Best Brands Consumer Products, Inc....

The Issue: Chemical Contamination; FDA analysis found product to contain methanol

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 29, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: IDArubicin Hydrochloride Injection USP 5gm/5mL (1mg/mL) for intravenous use...

The Issue: Presence of Particulate Matter: Product was found to contain silica and iron...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 29, 2022· Best Brands Consumer Products, Inc.

Recalled Item: The Mandalorian Hand Sanitizer Recalled by Best Brands Consumer Products,...

The Issue: Chemical Contamination; FDA analysis found product to contain benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2022· Preferred Pharmaceuticals, Inc.

Recalled Item: Preferred Pharmaceuticals Recalled by Preferred Pharmaceuticals, Inc. Due to...

The Issue: Out of specification results observed in dissolution during long term...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 28, 2022· Medminder Systems, Inc.

Recalled Item: MedMinder Medication Dispenser- Intended to serve as a medication reminder...

The Issue: Discontinuation of the Emergency Alert watch or pendant will no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2022· Stryker GmbH

Recalled Item: Smart Toe II Intramedullary Arthrodesis Implant Recalled by Stryker GmbH Due...

The Issue: The nickel-sensitivity statement on the outer carton may be partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Ortho-Clinical Diagnostics, Inc

Recalled Item: VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198...

The Issue: Falsely high or delayed patient and QC results may occur due to low end...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific Recalled by...

The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Ortho-Clinical Diagnostics, Inc

Recalled Item: VITROS Immunodiagnostic Products FSH Reagent Pack- IVD 1931922 Recalled by...

The Issue: Falsely high or delayed patient and QC results may occur due to low end...

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

Class II — Potential Health HazardOngoing