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 36461–36480 of 51,434 recalls
Recalled Item: STD KIT GK260 Recalled by Applied Medical Resources Corp Due to Applied...
The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver¿ 518RX Vascular Stent with Rapid Exchange Delivery System Recalled by...
The Issue: Manufacturing of the joint between the inner catheter and stylet of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Concerto Basic Shower Trolley is intended for assisted hygiene care...
The Issue: Reports of the bolts connecting the stretcher to the hydraulic piston and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog...
The Issue: The Mallinckrodt (Therakos) post-market monitoring process detected an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry Systems Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Increased U90-382 or...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Corporation Englewood Due to All lots of RAPIDFILL...
The Issue: All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Preservation System Signature Series PreBent Burs under the following...
The Issue: Metal shavings released from burs during use are due to contact between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL GBS Medium 20 ml in 100x15mm plate (Standard Petri Dish) Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fukuda Denshi patient monitor model DS-8100M and DS-8100N. The Fukuda...
The Issue: A possible malfunction where a Short-term Battery Error message has appeared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL- GBS Medium (Broth 3 ml Fill 13 x 100 mm Screw Cap Tube Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chocolate Marshmallows Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Original Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy and milk (butter declared).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Wowza Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy; and undeclared milk (cream declared).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Cashew Cow Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared sub-ingredient soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Holiday 4 pack Candy Bars Recalled by Zingerman's Candy Manufactory...
The Issue: Product recalled due to undeclared soy; and undeclared allergen milk (cream...
Recommended Action: Do not consume. Return to store for a refund or discard.