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. 2,684 recalls have been distributed to New Jersey in the last 12 months.
Showing 20961–20980 of 29,496 recalls
Recalled Item: BIOGRAPH mCT Flow Edge-3R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 16 TruePoint TV Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH 40 - 3 Ring Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH 40 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streamline OCT Occipito-Cervico-Thoracic System Recalled by RTI Surgical,...
The Issue: Potential for a product defect where the cannula may be obstructed. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...
The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...
The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX 16-slice whole body computed tomography X-ray system. Imaging diagnostic...
The Issue: The following issues have been found in MX 16-slice systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX 16-slice SKD whole body computed tomography X-ray system. Imaging...
The Issue: The following issues have been found in MX 16-slice systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acorn 130 Stairlift Recalled by Acorn Stairlifts, Inc Due to The design of...
The Issue: The design of the seats did not consistently have the adequate strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional Recalled...
The Issue: The Surgical Table Cushion (HybriGel Pads) could potentially contain staples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radionuclide Radiation Therapy System Product The product is a teletherapy...
The Issue: The latches of the frame adapter can be locked even if the locating pins of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VITROS¿ Chemistry Products Calibrator Kit 31 Recalled by Ortho-Clinical...
The Issue: There is an incorrect value (data/calibration mathematics) on ADDs. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm Three-fluted drill bit Recalled by Synthes (USA) Products LLC Due to...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.