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. 2,669 recalls have been distributed to New Jersey in the last 12 months.
Showing 22801–22820 of 29,496 recalls
Recalled Item: GEMINI TF 64 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iovera 155 Smart Tip Recalled by Myoscience Inc Due to The expiration date...
The Issue: The expiration date on the outer box label and the pouch label for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI GXL 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems Recalled...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujinon/Fujifilm Processor EPX 2500 Operation Manual. For use in endoscopic...
The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Acetaminophen reagents Recalled by Siemens Healthcare...
The Issue: A change in the concentration of N-acetylcysteine (NAC) that may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...
The Issue: Software anomaly may occur during the installation of an Assay Data Diskette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSW 1203.U/1 Recalled by BIOTRONIK, Inc. Due to Ventricular packing: LV...
The Issue: Ventricular packing: LV software programming versions for BIOTRONIK CRT-P...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Processor EPX 2500 High Definition Endoscopy Recalled by Fujifilm...
The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: in case a system error occurs and the system enters the "Bypass Fluoro" mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathoDx Strep B Grouping Latex Recalled by Remel Inc Due to A reagent...
The Issue: A reagent present may produce weak or slow reactions; continued use may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathoDx Strep Grouping Kit Recalled by Remel Inc Due to A reagent present...
The Issue: A reagent present may produce weak or slow reactions; continued use may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q systems Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists for a large amount of liquid to seep through the top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vancomycin Screen Agar Recalled by Becton Dickinson & Co. Due to The...
The Issue: The affected expired lots of product may have exhibited breakthrough growth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterococcus Screen Agar QUAD Plate Recalled by Becton Dickinson & Co. Due...
The Issue: The affected expired lots of product may have exhibited breakthrough growth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis zee systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The possibility exists for a large amount of liquid to seep through the top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are...
The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OxiMax N-65 Handheld Pulse Oximeter. N65 Recalled by Covidien LP (formerly...
The Issue: Potential missing segments on the display that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.