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. 2,503 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,503 in last 12 months

Showing 1470114720 of 27,462 recalls

Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Luminex Corporation

Recalled Item: VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as...

The Issue: Potential to lead to a false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2018· Roche Diagnostics Corporation

Recalled Item: CoaguChek¿ XS System Prothrombin time test: CoaguChek XS PT Test 2X24 Strips...

The Issue: Abnormally high INR test results with the affected CoaguChek test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 13, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System Recalled...

The Issue: The service manual was not updated at the time of the release of software...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· CMP Industries, Llc

Recalled Item: IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1 Recalled by CMP...

The Issue: Foreign material in product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 3000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 1000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 2000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 500 mL - Product Usage: Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· CMP Industries, Llc

Recalled Item: Technoflux IMPAK Resina lfquida acrilica elastic Curado-Calor Tipo 1...

The Issue: Foreign material in product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Howmedica Osteonics Corp.

Recalled Item: Tritanium TL Steerable Inserter Recalled by Howmedica Osteonics Corp. Due to...

The Issue: The firm received complaints related to the locking mechanism on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: B105/125 Patient Monitor. The device is a portable multiparameter unit...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: B20i Patient Monitor and B20i V2 Patient Monitor. The device Recalled by GE...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: PROCARE B20 Patient Monitor Recalled by GE Healthcare, LLC Due to Patient...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: PROCARE B40 Patient Monitor Recalled by GE Healthcare, LLC Due to Patient...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· TiSport, Llc

Recalled Item: TiLite X-Short anti-tip tubes Recalled by TiSport, Llc Due to The anti-tip...

The Issue: The anti-tip tubes potentially fail in certain situations and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: B40i Patient Monitor and B40i Patient Monitor V3 The device Recalled by GE...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: ACCOLADE Pacemaker Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: ESSENTIO Pacemaker Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing