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. 2,509 recalls have been distributed to Colorado in the last 12 months.
Showing 27261–27280 of 28,964 recalls
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The...
The Issue: Philips HeartStart XL+ Defibrillator/Monitor may become locked out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Isoline Implantable Defibrillation Lead Recalled by Sorin Group USA, Inc....
The Issue: Isoline defibrillation leads distributed may have internal insulation breach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bacterin Elutia Recalled by Bacterin International, Inc. Due to A portion of...
The Issue: A portion of a silicone wound drain was found to be cracked.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...
The Issue: Some devices had broken through the seal of the sterile pouch. ConMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian Eclipse Treatment Planning System for Radiotherapy Recalled by Varian...
The Issue: The calculation of dose dynamic plans containing different energy fields is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical C-Series Carry Bar Recalled by Prism Medical Services USA Due...
The Issue: The firm replaced the recalled carry bar with a plastic insert with a carry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proplege Coronary Sinus Catheter model PR9 Recalled by Edwards Lifesciences,...
The Issue: Edwards Lifesciences is recalling certain Proplege Coronary Sinus Catheter,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY TINGLING JELLY Personal Lubricant. The product is packaged into Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 700 Series Ventilators (PB740 and PB760) PB700 Series...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD System Recalled by Cenorin, LLC Due to The temperature sensor/control...
The Issue: The temperature sensor/control system in the HLD Systems Model 610 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by...
The Issue: Firm was made aware of incidents relating to the difficulty of properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000I Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000 Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Recalled by...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgG Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USHER¿ Support Catheter- Angled Tip WL130cm Recalled by Bard Peripheral...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROSHEATH¿ - 0.066 (1.7mm) proximal Recalled by Bard Peripheral Vascular...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.