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. 2,510 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,510 in last 12 months

Showing 1250112520 of 27,462 recalls

Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code: 303063 Recalled by...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Anti-HAV IgM assay-for the in vitro qualitative detection of...

The Issue: Current software version of the Anti-HAV IgM APP-file (version 06.05-101)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2019· Bard Peripheral Vascular Inc

Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The...

The Issue: During the firm's review of May 2019 complaint data, a significant increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2019· Conformis, Inc.

Recalled Item: iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 -...

The Issue: Medial and lateral polyethylene inserts did not securely fit into the cobalt...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...

The Issue: Sterile packaging incomplete seals may compromise sterility of the product

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2019· Abbott GmBH & Co. KG

Recalled Item: Alinity c Carbon Dioxide Reagent Kit Recalled by Abbott GmBH & Co. KG Due to...

The Issue: Abbott internal studies have determined that atmospheric Carbon Dioxide...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to The firm...

The Issue: The firm received complaints that the EMPOWR Acetabular Impactor Balls were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Steris Corporation

Recalled Item: Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer...

The Issue: The locking pin of the front wheel asse mbly of the Evolution Transfer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Steris Corporation

Recalled Item: Eagle 3000 Sterilizer Recalled by Steris Corporation Due to Potential for...

The Issue: Potential for the incorrect pressure safety valve being included in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Edwards Lifesciences, LLC

Recalled Item: EZ Glide Aortic Cannula Recalled by Edwards Lifesciences, LLC Due to Their...

The Issue: Their is a possibility that the cannula may separate from its connector,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: DxM 1096 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing