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. 2,753 recalls have been distributed to New Jersey in the last 12 months.
Showing 15381–15400 of 29,496 recalls
Recalled Item: TriMed Peg Guide Extender Recalled by TriMed Inc. Due to The spring on the...
The Issue: The spring on the PEG-Extender can rust due to the type of steel used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Locking Drill Guide Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Hex Driver 1.2 Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Wrist Hook Dorsal Impactor Recalled by TriMed Inc. Due to The WHD/WHV...
The Issue: The WHD/WHV impactors can rust over time due to an improper manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...
The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience has...
The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to There is a...
The Issue: There is a possibility that the liquid suction pump on some AIA-2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Thermal Chamber Motor Cable located in the following models:...
The Issue: Thermal chamber motors have electrical cables with single insulation rather...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT: a) S(64)-3R Recalled by Siemens Medical Solutions USA, Inc....
The Issue: The terminals on the plug may become loose and overheat.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph Horizon a) 3R Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: The terminals on the plug may become loose and overheat.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2 Anesthesia System. Sold under the following product names: AISYS...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer: In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime. In vitro diagnostic testing of clinical...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation...
The Issue: An incorrect display of the Biopsy Depth Gauge graphical representation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCEA Kit ASV Yellow Stripe Microbore Recalled by Becton Dickinson & Company...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TB Series Bipolar Pacing Leads Recalled by Oscor, Inc. Due to During the use...
The Issue: During the use of some TB - Temporary Bipolar Pacing Leads, featuring the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.