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. 2,448 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,448 in last 12 months

Showing 1914119160 of 27,462 recalls

Medical DeviceJuly 11, 2016· Bausch & Lomb Inc Irb

Recalled Item: Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED Recalled by Bausch & Lomb Inc...

The Issue: Possible dull knife edge

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Bausch & Lomb Inc Irb

Recalled Item: Laseredge 1.1mm Arrow Knife Angled Recalled by Bausch & Lomb Inc Irb Due to...

The Issue: Possible dull knife edge

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....

The Issue: The product lot failed to meet QC acceptance criteria during stability...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Home Monitoring System Model Number: 0200432 Recalled...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: INRatio Prothrombin Time (PT) Monitoring System Model Number: 0100007...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR Test Strips Model Number: 0100071 Recalled by Alere San...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· American National Mfg Inc

Recalled Item: Panacea Air Pro Mattress Control Unit Recalled by American National Mfg Inc...

The Issue: The Panacea Air Pro Mattress Control Unit is being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Testing System Model Number: 0200431...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio/ INRatio2 PT/INR Test Strips Model Number: 99007EU Recalled by...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR System Professional Model Numbers: 0100004 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Floor Mounting Column TS 7500 U Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Operating Table TruSystem 7000 U Recalled by Trumpf Medical Systems, Inc....

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Mobile Column TruSystem 7500 Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Stationary Column TruSystem 7599 Recalled by Trumpf Medical Systems, Inc....

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Argon Modified Flat l Electrode 28CM Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Straight Spatula Electrode 28CM Item Code: E278028...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic AP Argon Blunt Needle Electrode 28cm Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing