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. 2,794 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,794 in last 12 months

Showing 1126111280 of 13,536 recalls

DrugNovember 14, 2014· Attix Pharmaceuticals

Recalled Item: Hydralazine HCl active pharmaceutical ingredient packaged in varying grams...

The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2014· Attix Pharmaceuticals

Recalled Item: Isoproterenol Hydrochloride active pharmaceutical ingredient packaged in...

The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2014· Attix Pharmaceuticals

Recalled Item: Meloxicam active pharmaceutical ingredient packaged in varying grams or kg...

The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2014· Attix Pharmaceuticals

Recalled Item: Droperidol active pharmaceutical ingredient packaged in varying grams or kg...

The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2014· Attix Pharmaceuticals

Recalled Item: Bromocriptine Mesylate active pharmaceutical ingredient packaged in varying...

The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2014· Attix Pharmaceuticals

Recalled Item: Azithromycin Dihydrate active pharmaceutical ingredient packaged in varying...

The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2014· Attix Pharmaceuticals

Recalled Item: Miltefosine active pharmaceutical ingredient packaged in varying grams or kg...

The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2014· Chaotic Labz

Recalled Item: MAYHEM capsules Recalled by Chaotic Labz Due to Undeclared Dexamethasone

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

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2014· Fresenius Kabi USA, LLC

Recalled Item: GENTAMICIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Defective...

The Issue: Defective Container: Vials may be missing stoppers.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2014· Reckitt Benckiser LLC

Recalled Item: Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg) Recalled by...

The Issue: Defective container: A customer complaint revealed the presence of a...

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2014· Baxter Healthcare Corp.

Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Labeling: Label Error On Declared Strength: Bags of Potassium Chloride 10...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2014· Hospira Inc.

Recalled Item: Sterile powder Vancomycin Hydrochloride for Injection Recalled by Hospira...

The Issue: Correct Labeled Product Mispack: Product tray containing vials was...

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

Class III — Low RiskOngoing
Refund
DrugNovember 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful BEE POLLEN Recalled by Enterprises, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful INFINITY Recalled by Enterprises, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 30, 2014· Baxter Healthcare Corp.

Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection Recalled by Baxter...

The Issue: Subpotent Drug: Heparin raw material was found to have low potency

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2014· Hospira Inc.

Recalled Item: Meropenem I.V. 1 g is supplied in 30 mL injection vials Recalled by Hospira...

The Issue: Defective Container: Glass vials may crack due to low (thin) out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2014· CareFusion 213, LLC

Recalled Item: Scrub Care Chlorhexidine Gluconate Solution Recalled by CareFusion 213, LLC...

The Issue: Does Not Meet Monograph: Chlorhexidine Gluconate Surgical Scrub Brush is...

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

Class III — Low RiskOngoing
Refund
DrugOctober 22, 2014· Prometheus Laboratories Inc.

Recalled Item: Mercaptopurine Tablets Recalled by Prometheus Laboratories Inc. Due to...

The Issue: Failed Dissolution Specifications: Product found to be out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2014· Nanophase Technologies Corporation

Recalled Item: Z-COTE HP 1 TRANSPARENT ZINC OXIDE Recalled by Nanophase Technologies...

The Issue: cGMP Deviation; The incorrect amount of a raw material was added during the...

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

Class III — Low RiskOngoing
Refund
DrugOctober 17, 2014· Obagi Medical Products

Recalled Item: Obagi Nu-Derm Clear Recalled by Obagi Medical Products Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled...

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

Class II — Potential Health HazardOngoing
Refund