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. 1,791 recalls have been distributed to Colorado in the last 12 months.
Showing 46921–46940 of 51,434 recalls
Recalled Item: Medline Steam Biological Indicators Recalled by Steritec Products Mfc. Co.,...
The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years...
The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Afinity CQ2015A Intraocular Lens The visual correction of aphakia in...
The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Si Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Dual Camera Controller Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Instrument Control Box Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Si Surgeon Side Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597504110 Provisional AC ART SURF PROV 56/STR GRN 10 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90597003109 Articular Surface CR ART SURF 34/STR YEL 09MM Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 65595201201 Femur CR-FLEX POR HATCP FEM B-L Rx Recalled by Zimmer, Inc. Due...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597002009 Articular Surface CR ART SURF 12/PURPLE 9 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595601201 Femur CR-FLEX OPT FEM B-L Rx Sterile Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90597004109 Articular Surface CR ART SURF AE56/STR GRN 09MM Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90597002009 Articular Surface CR ART SURF 12/PURPLE 09MM Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597001303 Femur CR PRC FEM COMP SIZE CML Rx Recalled by Zimmer, Inc. Due...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597206126 Patella ALL POLY PAT COMP MICRO 26DIA Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597103110 Provisional CR ART SURF PROV 34/STR YEL 10 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595204110 Articular Surface XLPE CR ART SURF 5-6/STRGRN 10 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595202010 Articular Surface XLPE CR ART SURF 1 Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597003109 Articular Surface CR ART SURF 34/STRIPE YEL 9 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.