Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,383 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,383 in last 12 months

Showing 2430124320 of 27,462 recalls

Medical DeviceNovember 12, 2013· Ansell Sandel Medical Industries LLC

Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable...

The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2013· Ansell Sandel Medical Industries LLC

Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable...

The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2013· Ansell Sandel Medical Industries LLC

Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Long Disposable...

The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2013· Zimmer, Inc.

Recalled Item: Zimmer Trabecular Metal Total Ankle Talar Component Right Sizes 1-6 Recalled...

The Issue: As part of routine manufacturing process monitoring by Zimmer, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2013· Medtronic Advanced Energy, LLC

Recalled Item: Medtronic Advanced Energy Aquamantys3 Pump Generator Recalled by Medtronic...

The Issue: The internal protection circuitry on the electrosurgical output that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2013· Ansell Sandel Medical Industries LLC

Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable...

The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2013· Ansell Sandel Medical Industries LLC

Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Long Disposable...

The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2013· Ansell Sandel Medical Industries LLC

Recalled Item: Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable...

The Issue: Select lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008 Series Hemodialysis Machines: Models: 2008H Recalled by...

The Issue: 2008 Series Hemodialysis Machines complaints of saline bags inappropriately...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2013· Zimmer, Inc.

Recalled Item: Zimmer Trabecular Metal Total Ankle Tibial Base Component Sizes 1-6 Recalled...

The Issue: As part of routine manufacturing process monitoring by Zimmer, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2013· Sunrise Medical (US) LLC

Recalled Item: Sunrise Brand Zippie Voyage Recalled by Sunrise Medical (US) LLC Due to...

The Issue: There is a remote possibility for the plastic latch to deform over the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2013· Intuitive Surgical, Inc.

Recalled Item: Assembly Recalled by Intuitive Surgical, Inc. Due to Reports of friction...

The Issue: Reports of friction within certain instrument arms can interrupt smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100NX Recalled by Advanced Sterilization Products Due to Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2013· Advanced Sterilization Products

Recalled Item: STERRAD NX Recalled by Advanced Sterilization Products Due to Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2013· GE Healthcare, LLC

Recalled Item: Video Monitor Suspensions that may be on the following Fluoroscopic Recalled...

The Issue: Missing screws in the overhead Video Monitor Suspension. GE discovered that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2013· Biomerieux France Chemin De L'Or

Recalled Item: ZYM B Reagent () ZYM B reagent is an Recalled by Biomerieux France Chemin De...

The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2013· CareFusion 303, Inc.

Recalled Item: SmartSite Low Sorbing Infusion Set with Texium Close Male Luer Recalled by...

The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion Set with Texium...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2013· CareFusion 303, Inc.

Recalled Item: VersaSafe Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...

The Issue: CareFusion is recalling the VersaSafe Extension Intravascular Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2013· Biomerieux France Chemin De L'Or

Recalled Item: API NH () API NH is a standardized system Recalled by Biomerieux France...

The Issue: bioM¿rieux identified a visual defect and activity issue on the ZYM B...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2013· Baxter Healthcare Corp.

Recalled Item: IntelliFill i.v. Pharmacy Compounding Device (PCD). Intended to fill...

The Issue: Following a retrospective review for Baxter Daytona Complaint CR-954, it was...

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

Class II — Potential Health HazardOngoing