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. 2,551 recalls have been distributed to Colorado in the last 12 months.
Showing 21041–21060 of 51,434 recalls
Recalled Item: TherMax Blood Warmer Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: TherMax Blood Warmers may not be in compliance with an electrical safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ra Medical Systems DABRA Catheter 5F (1.5mm) Recalled by Ra Medical Systems,...
The Issue: The firm has become aware there is a potential problem with its DABRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVENCARE G3 Blood Glucose Test Strips Recalled by Medline Industries Inc Due...
The Issue: Incomplete seal and premature expiration of individually packaged Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE TITANIUM NON- FILLED Recalled by Angiodynamics Inc....
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Diff Dropper Recalled by Biomedical Polymers, Inc. Due to The metal...
The Issue: The metal cannula of the device either broke and the broken piece left in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the Recalled by...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemo-Drop Blood Dispenser Recalled by Biomedical Polymers, Inc. Due to The...
The Issue: The metal cannula of the device either broke and the broken piece left in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor Recalled by...
The Issue: Eversense Sensors have prematurely stopped functioning due to inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Behind-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XCELA Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to Snap...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC NON-FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.