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. 1,065 recalls have been distributed to Colorado in the last 12 months.
Showing 16401–16420 of 51,434 recalls
Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Unipedicular Cement Delivery Cannula Kit Recalled by Zavation Due...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10G SINGLE CEMENT DELIVERY KIT (5 FILLERS). For use in Recalled by Zavation...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVPlasty Recalled by Zavation Due to Products distributed as sterile may not...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Direct Access Diamond Tip Trocar Recalled by Zavation Due to...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL) Recalled by...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas Liat Analyzer: respiratory virus panel nucleic acid assay system...
The Issue: Invalid or false positive results for one or more targets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B assay cobas Liat- Reagents Recalled by...
The Issue: Invalid or false positive results for one or more targets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Model Number: (9A)9.0.0.113 Recalled by RAYSEARCH LABORATORIES AB...
The Issue: Flags edited in RayCare after a patient has been checked in may not always...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty 10G Recalled by Zavation Due to Products distributed as sterile may...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10G DIRECT SINGLE BONE ACCESS KIT. For use in Orthopedic / spinal...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended Recalled...
The Issue: BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel Recalled by...
The Issue: Aftermarket front bezel components were installed during service/repair, not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drop Arm Versamode" Recalled by Gf Health Products Due to The front casters...
The Issue: The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.