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. 1,139 recalls have been distributed to New Jersey in the last 12 months.
Showing 8921–8940 of 29,496 recalls
Recalled Item: Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls Recalled by MEDLINE...
The Issue: Affected product was shipped from the warehouse at room temperature instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Recalled by ROi CPS LLC Due to Kits lacks rubber latex warning label.
The Issue: Kits lacks rubber latex warning label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107...
The Issue: Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Recalled by...
The Issue: Due to: 1) Manufacturing issue that result in inaccurate force measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 -intended for dental...
The Issue: Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Infant Heel Warmer Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medichoice Infant Heel Warmer Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmers w/strap Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heel Snuggler Recalled by Philips North America Llc Due to After the device...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Proton Therapy...
The Issue: Proton Therapy System (PTS) software can be started in the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infa-Therm Transport Mattress Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBB-06 Hemodialysis Delivery System Recalled by Nikkiso Ltd - Shizuoka Plant...
The Issue: Device lacks premarket approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Pro Tibial Preparation Tray Recalled by Howmedica Osteonics Corp....
The Issue: Triathlon Pro Tibial Preparation Tray may have been kitted with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Radiotherapy System - System Label: "*** by Medical, Inc. Due to Due...
The Issue: Due to dose discrepancy when delivering a plan to a patient in a Non-HFS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Recalled by Philips North America Llc Due to Due to a...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Sensis Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software error which affects Sensis Vibe Hemo, Sensis and Sensis Vibe Combo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack Recalled...
The Issue: Lower than expected results for VITROS¿ Immunodiagnostic Products TSH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WIRION EMBOLIC PROTECTION SYSTEM Recalled by Cardiovascular Systems Inc Due...
The Issue: Under certain circumstances, the WIRION filter assembly may become difficult...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electri-Cool II Portable Cold Therapy Unit Recalled by Gentherm Medical, LLC...
The Issue: This recall has been initiated to provide a labeling update with revised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.