Product Recalls in Colorado
Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,152 recalls have been distributed to Colorado in the last 12 months.
Showing 6401–6420 of 28,964 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: 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: 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: 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: 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: 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: ICD-VR VISIA AF S US/OUS DF4 Recalled by Medtronic Inc., Cardiac Rhythm and...
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 CROME HF MRI IS1 DF1 Recalled by Medtronic Inc., Cardiac Rhythm and...
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: ICD CROME DR MRI IS1 DF1 Recalled by Medtronic Inc., Cardiac Rhythm and...
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: ICD-VR DVMD3D4 PRIMO MRI Recalled by Medtronic Inc., Cardiac Rhythm and...
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: CRT-D VIVA QUAD XT GOLD CTD Recalled by Medtronic Inc., Cardiac Rhythm and...
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.