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. 2,766 recalls have been distributed to New Jersey in the last 12 months.
Showing 14741–14760 of 29,496 recalls
Recalled Item: 14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow Disposable Cartridge Recalled by Vyaire Medical Due to Testing has...
The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow Disposable Cartridge with IV Extension Set Recalled by Vyaire Medical...
The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo Clinch II Auto Suture Grasper Recalled by COVIDIEN LLC Due to...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo Grasp Auto Suture Grasper 5mm The Recalled by COVIDIEN LLC Due...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure kits include devices from the affected lots distributed OUS...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truliant Tibial Fit Tray Cemented SZ 3F / 3T Recalled by Exactech, Inc. Due...
The Issue: 2.5 Truliant Fit Trays were mismarked as 3
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits Recalled...
The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS II SUTURE 18"(45CM) 2-0 VIO Product Code:Z739D - PDS Recalled by...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL Recalled by...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM)...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity Recalled by Elekta Limited Due to Users need to be aware when...
The Issue: Users need to be aware when using these protocols for daily on line plan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Xstar Slit Knife 2.4 mm Recalled by Beaver Visitec Due to Mislabeling
The Issue: Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...
The Issue: One of the software algorithms used to detect sample dispense errors was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Elements Software revisions of the RT Elements applications have Recalled...
The Issue: There is a potential for an incorrect dose distribution calculation by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Tibial Total Ankle Prosthesis Tray Recalled by Integra...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.