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. 2,786 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,786 in last 12 months

Showing 1324113260 of 13,536 recalls

DrugJune 7, 2012· Fougera Pharmaceuticals, Inc.

Recalled Item: Erythromycin Topical Solution USP Recalled by Fougera Pharmaceuticals, Inc....

The Issue: Chemical Contamination: This product is being recalled because trace amounts...

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

Class III — Low RiskOngoing
Refund
DrugJune 6, 2012· Meridian Medical Technologies a Pfizer Company

Recalled Item: Diazepam Injection Recalled by Meridian Medical Technologies a Pfizer...

The Issue: Impurities/Degradation Products: High Out of Specification levels for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2012· Watson Laboratories Inc

Recalled Item: Caziant (desogestrel and ethinyl estradiol) Tablets Recalled by Watson...

The Issue: Impurities/Degradation Products: High Out-of-specification results were...

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

Class III — Low RiskOngoing
Refund
DrugJune 5, 2012· Bristol-myers Squibb Company

Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...

The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2012· Bristol-myers Squibb Company

Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...

The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2012· JHP Pharmaceuticals, LLC

Recalled Item: Pitocin (Oxytocin Injection Recalled by JHP Pharmaceuticals, LLC Due to...

The Issue: Labeling: Label Mix-up: Pitocin storage conditions should be labeled, "Store...

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

Class III — Low RiskOngoing
Refund
DrugJune 4, 2012· GlaxoSmithKline Inc

Recalled Item: Trizivir (abacavir sulfate 300mg Recalled by GlaxoSmithKline Inc Due to...

The Issue: Adulterated Presence of Foreign Tablets: Trizivir 300/150/300 mg tables, Lot...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2012· Bracco Diagnostics Inc

Recalled Item: CARDIOGEN-82 (Rubidium Rb 82 Generator) Recalled by Bracco Diagnostics Inc...

The Issue: GMP deviation; Sr-82 levels exceeded alert limit specification

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2012· Bayer HealthCare Pharmaceuticals Inc.

Recalled Item: Leukine sargramostim 5 x 500 mcg/mL vial Recalled by Bayer HealthCare...

The Issue: Impurities/Degradation Products: A confirmed out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugMay 30, 2012· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate & Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL...

The Issue: Impurities/Degradation Products: exceeded specification at 3 month stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: CHORIONIC GONADOTROPIN (STANDARD) - 21 DAY 200 UNIT VIALS KIT 1 KIT Recalled...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: FOLIC ACID 10MG/ML INJECTABLE 60 ML (1 PRODUCT) Recalled by Franck's Lab...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Mallinckrodt Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...

The Issue: Subpotent (Multiple Ingredient) Drug: Low out of specification assay results...

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

Class III — Low RiskOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: EPINEPHRINE **(25X1ML AMPULS) 1:1000 1MG/ML INJECTABLE 25 ML Recalled by...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Mallinckrodt Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...

The Issue: CGMP Deviations: This product is being recalled because expired flavoring...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· The Menz Club, LLC

Recalled Item: V Maxx Rx Recalled by The Menz Club, LLC Due to Marketed Without An Approved...

The Issue: Marketed Without An Approved NDA/ANDA: Samples tested by FDA were found to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: ALPROSTADIL 10MCG/ML INJECTABLE 10 ML Recalled by Franck's Lab Inc., d.b.a....

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: AFLIBERCEPT Recalled by Franck's Lab Inc., d.b.a. Franck's Compounding Lab...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: CYCLOPENT/PHENYLEPH/TROPICAMIDE/PROPARACAINE 2%/2.5%/1%/0.5% OPHTHALMIC 5 ML...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: ENGERIX-B Recalled by Franck's Lab Inc., d.b.a. Franck's Compounding Lab Due...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund