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. 2,683 recalls have been distributed to New Jersey in the last 12 months.
Showing 22961–22980 of 53,621 recalls
Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Viral Panel RUO Recalled by Becton Dickinson & Co. Due to...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max GC RT PCR Assay Recalled by Becton Dickinson & Co. Due to The...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoject EI Recalled by Owen Mumford USA, Inc. Due to There is a possible...
The Issue: There is a possible assembly error on Autoject EI, lot number V14. This lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max MRSA Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 2 USA Recalled by Becton Dickinson & Co. Due to The foil...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Vaginal Panel Recalled by Becton Dickinson & Co. Due to The foil...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 2 EU LUO Recalled by Becton Dickinson & Co. Due to The...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Elecsys Anti-CCP Immunoassay Catalog # 05031656160 Recalled by Roche...
The Issue: Performance issues with certain lots of the Elecsys Anti-CCP assay on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion systems with software version R1.2 -Interventional...
The Issue: The cold restart of Azurion R1.2 systems may take up to 7 minutes if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Elecsys Anti-CCP Immunoassay Catalog # 07251670190 Recalled by Roche...
The Issue: Performance issues with certain lots of the Elecsys Anti-CCP assay on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The...
The Issue: Non-conforming devices are identified, which may not have been included in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fukushima suction tubes Recalled by TeDan Surgical Innovations LLC Due to...
The Issue: There was incorrect raw material used in the production of the identified lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...
The Issue: CGMP Deviations: product was manufactured that did not prevent possible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobazam Oral Suspension Recalled by Bionpharma Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: Out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...
The Issue: CGMP Deviations: product was manufactured that did not prevent possible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...
The Issue: CGMP Deviations: product was manufactured that did not prevent possible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...
The Issue: CGMP Deviations: product was manufactured that did not prevent possible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...
The Issue: CGMP Deviations: product was manufactured that did not prevent possible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.