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. 2,509 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,509 in last 12 months

Showing 2556125580 of 28,964 recalls

Medical DeviceNovember 20, 2013· SpineFrontier, Inc.

Recalled Item: Indus Invue Screws: IM71016-XX: 04.5mm Recalled by SpineFrontier, Inc. Due...

The Issue: Mismarked and unmarked screws

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· CooperVision Inc.

Recalled Item: ClearSight(TM) Toric 1 day (ocufilcon D) Recalled by CooperVision Inc. Due...

The Issue: Lots were labeled with incorrect expiration dates on secondary package...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· SpineFrontier, Inc.

Recalled Item: Indus Invue Screws: IM71058-XX: 04.2mm Recalled by SpineFrontier, Inc. Due...

The Issue: Mismarked and unmarked screws

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Hyperion Medical

Recalled Item: All brochures printed before November 20 Recalled by Hyperion Medical Due to...

The Issue: Brochures and web site information for the HyperBlue 1530 diode laser...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Boston Scientific Corporation

Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 1 configuration)...

The Issue: Sterility of device may be compromised due to lack of pouch seal integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Sorin Group Italia S.r.l.

Recalled Item: ORCHESTRA/ORCHESTRA PLUS Programmer Recalled by Sorin Group Italia S.r.l....

The Issue: Sorin has voluntarily issued a notification to physicians related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Boston Scientific Corporation

Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 10 configuration)...

The Issue: Sterility of device may be compromised due to lack of pouch seal integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Boston Scientific Corporation

Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 5 configuration)...

The Issue: Sterility of device may be compromised due to lack of pouch seal integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Boston Scientific Corporation

Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 5 configuration)...

The Issue: Sterility of device may be compromised due to lack of pouch seal integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· SpineFrontier, Inc.

Recalled Item: Indus Invue Screws: lM71059-XX: Indus Screw 04.2mm SelfDrilling. Used to...

The Issue: Mismarked and unmarked screws

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· SpineFrontier, Inc.

Recalled Item: Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling. Used to...

The Issue: Mismarked and unmarked screws

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2013· Boston Scientific Corporation

Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 10 configuration)...

The Issue: Sterility of device may be compromised due to lack of pouch seal integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution CR Articular Surface Provisional-Purple 9mm...

The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Porous Patella Drill Guide-29mm dia./10mm...

The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Ultradent Products, Inc.

Recalled Item: Opal Orthodontics by Ultradent. Avex CX2 Ceramic Orthodontic Brackets Avex...

The Issue: Ultradent Products Inc. is recalling various lots of Avex CX2 Orthodontic...

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

Class III — Low RiskOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 110cm tubing & 13mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Conset Infusion Set with tubing & 9mm cannula packaged in 5-packs...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Conset Infusion Set with 60cm tubing & 6mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing