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. 1,868 recalls have been distributed to Colorado in the last 12 months.
Showing 34361–34380 of 51,434 recalls
Recalled Item: Integrated Food Service Egg & Cheese Bagel Thin Sandwich Code #C38004/380004...
The Issue: Potential Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cafe Favorites Turkey Ham & Cheese Submarine Code #C02184/02184 Recalled by...
The Issue: Potential Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Integrated Food Service Chili Cheese Dog Whole Grain Hot Dog Bun Recalled by...
The Issue: Potential Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nitrofurantoin Oral Suspension Recalled by Nostrum Laboratories, Inc. Due to...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lodrane D (Brompheniramine maleate 4 mg and Pseudoephedrine HCl 60 mg)...
The Issue: Labeling: Not Elsewhere Classified: correctly labeled bottles were packaged...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Left Foot/20mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Left Foot/30mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OT1000 Series Orthopedic Surgical Tables Recalled by Steris Corporation Due...
The Issue: STERIS has identified that the pivot pin assembly located on the table top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Right Foot/30mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy...
The Issue: Presence of leaks near top of the PrismaSate bags
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Proximal Foot/Right Recalled by Synthes (USA)...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV3 EverFiex" Self-expanding Peripheral Stent System Recalled by Ev3, Inc....
The Issue: Medtronic is issuing a medical device recall to return product potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Right Foot/20mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Proximal Foot/Left Recalled by Synthes (USA)...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...
The Issue: The affected K-wires do not meet specification requirements. Specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiesse (+) Lidocaine Recalled by Merz North America, Inc. Due to...
The Issue: Complaints reported of Radiesse (+) unable to be expelled from the syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz....
The Issue: Product did not meet specifications for Zinc Acetate (OOS).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.