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. 2,471 recalls have been distributed to Colorado in the last 12 months.
Showing 37321–37340 of 51,434 recalls
Recalled Item: Screenses Color Sunscreen Recalled by Sesderma, SL Due to cGMP Deviations;...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Salises Facial Moisturizing Acne Treatment Gel Recalled by Sesderma, SL Due...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Repaskin 50 (octocrylene 7% Recalled by Sesderma, SL Due to cGMP Deviations;...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Repaskin 30 (octacrylene 4% Recalled by Sesderma, SL Due to cGMP Deviations;...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Screenses Color Sunscreen Tinted facial make-up compact Recalled by...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Repaskin 30 (octacrylene 4% Recalled by Sesderma, SL Due to cGMP Deviations;...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dryses Aluminum Chlorohydrate Deodorant for Women Recalled by Sesderma, SL...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Repaskin 50 (octocrylene 7% Recalled by Sesderma, SL Due to cGMP Deviations;...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dryses Aluminum Chlorohydrate Deodorant for Men Roll-on Recalled by...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dryses Aluminum Chlorohydrate Antiperspirant Solution Recalled by Sesderma,...
The Issue: cGMP Deviations; product does not comply with cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...
The Issue: Complaint investigation concluded that although product quality requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Granny Smith green apples Recalled by Del Monte Fresh Produce N.A.,...
The Issue: Apples have the potential to be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...
The Issue: The defective component can cause gas leakage through the device. This can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SSS Reprocessed Zimmer Recalled by Stryker Sustainability Solutions Due to...
The Issue: It was reported that packaging was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...
The Issue: The following MRx software issue has been identified: MRx model M3535A with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus...
The Issue: The IFU of the Neptune Plus Pads, does not match that submitted in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.