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. 1,983 recalls have been distributed to Delaware in the last 12 months.
Showing 6261–6280 of 27,373 recalls
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline O.R. Scissors Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: The scissors were manufactured without a tip protector resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Driver Instrument Recalled by Boston Scientific Neuromodulation Corporation...
The Issue: Pending update to indirect decompression system instructions for use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Icelock 125 Ratchet Recalled by Ossur H / F Due to A mechanical lock used to...
The Issue: A mechanical lock used to connect and release a locking liner into a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...
The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-VR DVMC3D1 EVERA MRI S OUS/US DF1 Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRTD COBALT HF QUAD MRI IS4 DF1 Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRTD DTMA2D4 CLARIA MRI OUS DF4 Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRTD DTMA1D1 CLARIA MRI US DF1 Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.