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. 2,841 recalls have been distributed to New Jersey in the last 12 months.
Showing 5381–5400 of 53,621 recalls
Recalled Item: BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics...
The Issue: There is a potential risk that the image colony count does not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi NAV Suction Recalled by Integra LifeSciences Corp. Due to Specific...
The Issue: Specific lots of TruDi NAV Suction Instruments 0 Degrees were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fox's u-bet Vanilla Flavored Syrup Recalled by SUBCO FOODS INC Due to...
The Issue: Customer complaint for bloated bottles. Testing and examination of these...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fox's u-bet Sugar-Free Chocolate Flavored Syrup Recalled by SUBCO FOODS INC...
The Issue: Customer complaint for bloated bottles. Testing and examination of these...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nitrofurantoin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GM60A. Digital Diagnostic Mobile X-Ray System. Recalled by NeuroLogica...
The Issue: Potential for the anti-fall system of the device arm to fail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235 ProteusPLUS and ProteusONE Recalled...
The Issue: Safety Parameters Verification Mechanisms can be deactivated in clinical runtime
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013...
The Issue: Invalid Controls. The Low Control is out of range; too high which causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM...
The Issue: During the assembly of the FRT250 cartridge assembly, an incorrect component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2 Recalled by...
The Issue: It was confirmed that fibrinogen in patient plasma samples precipitates out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for...
The Issue: Devices were labeled with an expiration date of four years and ten days...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B-Intended to be used Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The recalled product is mis-labeled as Ancient Grain + Vegetable Recalled by...
The Issue: Undeclared Almond and Soy. The Grain + Celery Salad with Apple Cider...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lidocaine HCL Injection Recalled by TAILSTORM HEALTH INC Due to Subpotent...
The Issue: Subpotent Drug: reduced efficacy for epinephrine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Decitabine for Injection 50mg per vial Recalled by SUN PHARMACEUTICAL...
The Issue: CGMP Deviations: Out of Specification for Total Aerobic Microbial Count...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PEG-3350 Recalled by Novel Laboratories, Inc. d.b.a Lupin Somerset Due to...
The Issue: Defective container: potential for non-sealed pouches which can lead to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Micafungin for injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Cross contamination with other products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.