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. 2,522 recalls have been distributed to Colorado in the last 12 months.
Showing 24961–24980 of 28,964 recalls
Recalled Item: ENT PRGM 9734636 ADD FUSION NAV AxiEM Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8" Circle Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUMOR RES. PACK 9733553 AxiEM S.M. Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4.5" Circle Reorder Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRAPE 9732722 TUBE STERILE O-ARM 20PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UPGRD PRGM 9734638 ADD AxiEM NAVIGATION Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Recalled by Davol,...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Aera magnetic resonance system. Indicated for use as a Recalled by...
The Issue: Siemens discovered a processing error for the MAGNETOM Aera magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4"x6" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated PD systems are used in the treatment Recalled by...
The Issue: System error 01779 is produced when the battery cannot be charged due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUMOR RESECTION KIT 9733608 SKULL MOUNT Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INST 9731132 KIT CR DRIVER 5PK Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPSY NEEDLE KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAK 9733497 NAV NIM-SPINE PEDICLE ACC KT Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATIENT TRACKER 9733534XOM ENT 1PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and...
The Issue: Potential malfunction due to a software issue for ACUSON SC2000 ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia E camera system. Emission Computed Tomography System used to Recalled...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump model 8100 with software version 9.1.18 and software Recalled by...
The Issue: CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.