Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,017 recalls have been distributed to Delaware in the last 12 months.
Showing 16981–17000 of 48,330 recalls
Recalled Item: IceSeed" Prostate Cryoablation Kit Recalled by Boston Scientific Corporation...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Three IcePearl" 2.1 CX Prostate Cryoablation Kit Recalled by Boston...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) Recalled by Becton...
The Issue: BD has confirmed the presence of blood on the cannulas of the BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed" 1.5 MRI Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IcePearl" 2.1 CX 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSphere" 1.5 Cryoablation Needle Recalled by Boston Scientific Corporation...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceRod" 1.5 MRI Cryoablation Needle¿ Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceFORCE" 2.1 CX Prostate Cryoablation Kit Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceRod" 1.5 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Three IceFORCE" 2.1 CX Prostate Cryoablation Kit Recalled by Boston...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSphere" 1.5 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
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: 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: Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Recalled by Fresenius...
The Issue: Cross Contamination with other products: trace amounts of lidocaine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.