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. 1,777 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,777 in last 12 months

Showing 4830148320 of 53,621 recalls

Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: CPT¿ Femoral Stem (CPT 12/14 STEM SIZE 0 COCR Recalled by Zimmer, Inc. Due...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: Sidus" Head (Not distributed in the United States) Recalled by Zimmer, Inc....

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: Multipolar¿ Bipolar Cup METAL SHELL 38 MM OD through 71 Recalled by Zimmer,...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Zimmer, Inc.

Recalled Item: CoCr Head (Not distributed in the United States) Used in Recalled by Zimmer,...

The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· CareFusion 303, Inc.

Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion Set, Model#...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Stryker Endoscopy

Recalled Item: Stryker Vision Mounting Arm Recalled by Stryker Endoscopy Due to When...

The Issue: When positioning the display located on top of the video cart, it is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2013· Implantech Associates Inc

Recalled Item: Device Name: Terino Square Chin-Style II-Medium Recalled by Implantech...

The Issue: Implantech initiated a voluntary recall of certain lots of Terino Square...

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

Class II — Potential Health HazardOngoing
DrugAugust 30, 2013· Boehringer Ingelheim Roxane Inc

Recalled Item: SPIRIVA HandiHaler (Tiotropium Bromide Inhalation Powder) Capsules 18 mcg...

The Issue: Presence of Foreign Substance: This recall is being conducted due to the...

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

Class III — Low RiskOngoing
Refund
DrugAugust 30, 2013· Hospira Inc.

Recalled Item: Aminosyn II Recalled by Hospira Inc. Due to Presence of Particulate Matter:...

The Issue: Presence of Particulate Matter: Confirmed customer complaint of particulate...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 30, 2013· Watson Laboratories Inc

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Watson...

The Issue: Defective Container: Defective bottles may not have tamper evident seals...

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

Class III — Low RiskOngoing
Refund
DrugAugust 29, 2013· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU (TM) IBUPROFEN Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Labeling: Incorrect or missing lot and/or exp date- This product is being...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Procter & Gamble Co

Recalled Item: Vicks NyQuil Cold and Flu Nighttime Relief Recalled by Procter & Gamble Co...

The Issue: Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Hospira Inc.

Recalled Item: 5% Lidocaine HCl and 7.5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter; report of visible particulates in the glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2013· Cubist Pharmaceuticals, Inc.

Recalled Item: Cubicin (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter; Glass particulates observed in vials

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: CARESTREAM DRX -Mobile Retrofit Kit Recalled by Carestream Health Inc. Due...

The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...

The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...

The Issue: It was discovered that Carestream received a report from a customer that 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to The...

The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...

The Issue: Updated Instructions for Use: Bloodline connections not tightened per...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2013· Vital Diagnostics, Inc.

Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...

The Issue: High positive calcium bias on plasma sample versus results on serum

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

Class II — Potential Health HazardOngoing