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.

51,434 total recalls
2,522 in last 12 months

Showing 2492124940 of 28,964 recalls

Medical DeviceApril 30, 2014· Microport Orthopedics INC.

Recalled Item: PATH(R) THREAD CUP ADAPTOR Recalled by Microport Orthopedics INC. Due to...

The Issue: Difficulty removing the cup adaptor from the impaction handle during surgery

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2014· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. Merge Hemo monitors Recalled by Merge Healthcare, Inc....

The Issue: The application may crash during the cath lab procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2014· Mako Surgical Corporation

Recalled Item: Robotic Arm Interactive Orthopedic System (RIO) Recalled by Mako Surgical...

The Issue: Revision of the field manual

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2014· Synthes, Inc.

Recalled Item: Synthes ProDisc-C 2.0mm Milling Bit Recalled by Synthes, Inc. Due to Certain...

The Issue: Certain lots of the ProDisc-C 2.0mm Milling Bits have an increased potential...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2014· Convatec Inc.

Recalled Item: Convatec Flexi Seal Control Fecal Management System Rx Only by Convatec Inc....

The Issue: Convatec Inc. is recalling Flexi-seal FMS Control Kit since it does not have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 28, 2014· Greatbatch Medical

Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...

The Issue: Greatbatch identified that the documentation does not support the five-year...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2014· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Connection issues between the PD transfer set catheter connector and an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...

The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Hitachi Medical Systems America Inc

Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...

The Issue: The firm received a complaint stating the Coil Extension Cable accessory...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· CryoLife, Inc.

Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...

The Issue: Serum albumin component monomer failed to meet internally established end of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PIN 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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: DISP 9730950 STRL SPHERE 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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: INSTRUMENT TRACKER 9733533XOM 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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PIN 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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: BAG 9732315 MOUSE STERILE 15 PK Recalled by Medtronic Navigation, Inc. Due...

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: PACK 9731975 TUMOR RESECTION AXIEM CR 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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: DISP 9730951 STRL SPHERE 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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Cenorin, LLC

Recalled Item: HLD Systems Model 610 Washer/High Level Disinfector. Maximum weight of...

The Issue: Cenorin LLC is voluntarily recalling HLD Systems Model 610 Washer/High Level...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing