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. 942 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
942 in last 12 months

Showing 50361–50380 of 53,621 recalls

DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Quadmix Injection Recalled by Pallimed Solutions Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Diazepam Injectable Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Nandrolone Decanoate Injectable Recalled by Pallimed Solutions Due to Lack...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Tacrolimus Ophthalmic Recalled by Pallimed Solutions Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Hydroxyprogesterone CAPR.(G.S.) Recalled by Pallimed Solutions Due to Lack...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Verapamil Injection Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Testosterone Cypionate/Testosterone Enanthate Injection Recalled by Pallimed...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Atropine Injection Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: DMSO Aqueous Irrigation 50% Recalled by Pallimed Solutions Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2013· Actavis South Atlantic LLC

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) 300 mg Recalled by...

The Issue: Failed USP Dissolution Test Requirements: Out-of-specification dissolution...

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2013· Watson Laboratories, Inc.-(Actavis) - Florida

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...

The Issue: Failed Tablet/Capsule Specifications: Broken tablets

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2013· Actavis Inc

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Broken tablets

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...

The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...

The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD ONE VIOLET AND ONE BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC)...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 200 Sterilization System Recalled by Advanced Sterilization Products...

The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100NX Sterilization System Recalled by Advanced Sterilization...

The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...

The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...

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

Class III — Low RiskOngoing