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. 2,787 recalls have been distributed to New Jersey in the last 12 months.
Showing 11941–11960 of 29,496 recalls
Recalled Item: RayStation 9A Recalled by RAYSEARCH LABORATORIES AB Due to Software error...
The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.0 to RayStation 5 Service Pack 2 - Product Recalled by...
The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 6 Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens IMMULITE 2000 XPi Immunoassay System - In vitro Chemistry Recalled...
The Issue: Flexible tubing connected to the liquid waste bottle can crack during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) CentraLink Data Management System software version 16.0.2 Siemens...
The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIRECT SUPPLY Attendant VITAL SIGNS MONITOR Recalled by Mediana Co., Ltd....
The Issue: Failures were found in the temperature measurement function while in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer...
The Issue: Flexible tubing connected to the liquid waste bottle can crack during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Atellica Data Manager software version 1.0 Siemens Material Number...
The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250i Recalled by Mevion Medical Systems, Inc. Due to Couch...
The Issue: Couch Correction moves sent after using a 3D CT scan are partially lost if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3COR DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due to...
The Issue: Lack of pouch seal. Product is labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK GUIDE SLEEVE 3.2MM...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 14 HOLE 234MM...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE LEFT 14 HOLE 227MM...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 6.5 Cannulated Screw Tap - Bone fixation screw Recalled by Biomet Due...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.