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. 1,063 recalls have been distributed to Colorado in the last 12 months.
Showing 21541–21560 of 51,434 recalls
Recalled Item: Clotrimazole and Betamethasone Dipropionate Cream USP Recalled by Glenmark...
The Issue: Temperature Abuse: Complaints received of liquidy texture.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM - Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Jarit GEMINI CLAMP 9 1/4 inch - used in Recalled by Integra...
The Issue: A small crack at the box lock corner may after multiple cleaning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard Recalled by Arrow...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Recalled by...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuardian Heart Remote Monitoring Kit Recalled by Preventice Services,...
The Issue: The device data being collected and transferred to the monitoring center may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp Recalled by Zimmer...
The Issue: The potential that the end of the shaft could fail to effectively mate with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Short Fill: fill...
The Issue: Short Fill: fill volume was out of specification at 94 mL (specification: no...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amy's Bowls - Broccoli & Cheddar Bake Recalled by Amys Kitchen Inc Due to...
The Issue: Consumer complaints of black plastic found in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FROZEN VAN YOG Recalled by Belfonte Ice Cream & Dairy Foods Co Due to...
The Issue: Undeclared allergens peanuts: Peanut butter ice cream was placed in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PreGel Lemon 50 4.4 lb (2kg) bag Recalled by PreGel America, Inc. Due to...
The Issue: Undeclared Milk. The firm received a complaint that there was milk in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sandia Rose Recalled by Milkweed & Monarch, LLC Due to Potential Salmonella...
The Issue: recalling certain lots of Ginger Spice, Sandia Rose, and Honey Lavender teas...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honey Lavender Recalled by Milkweed & Monarch, LLC Due to Potential...
The Issue: recalling certain lots of Ginger Spice, Sandia Rose, and Honey Lavender teas...
Recommended Action: Do not consume. Return to store for a refund or discard.