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. 2,794 recalls have been distributed to New Jersey in the last 12 months.
Showing 10941–10960 of 29,496 recalls
Recalled Item: MH-200S Recalled by Shimadzu Medical Systems Due to The firm has identified...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bransist Safire Recalled by Shimadzu Medical Systems Due to The firm has...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinias Recalled by Shimadzu Medical Systems Due to The firm has identified...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...
The Issue: A software error was detected within software version 1.3.4 for the Tempus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...
The Issue: Zimmer Biomet is conducting a medical device correction to update the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Set Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centeze Centesis Catheter Recalled by Galt Medical Corporation Due to Due to...
The Issue: Due to a manufacturing issue, the catheter tip geometry is incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream 35 Portable Respiratory Monitor Recalled by Covidien Llc Due to...
The Issue: The firm has released software update V01.05.02.16 (also known as V1.5.2) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Cobalt DR MRI SureScan DDPB3D1 Recalled by Medtronic Inc., Cardiac...
The Issue: Under rare circumstances, the component may be susceptible to a failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Cobalt HF CRT-D MRI SureScan DTPB2D1 Recalled by Medtronic Inc.,...
The Issue: Under rare circumstances, the component may be susceptible to a failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic COBALT HF QUAD CRT-D MRI SureScan Recalled by Medtronic Inc.,...
The Issue: Under rare circumstances, the component may be susceptible to a failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.