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. 1,072 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,072 in last 12 months

Showing 7641–7660 of 48,219 recalls

Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Pediatric Urology Wolson Pack Recalled by American Contract Systems, Inc....

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Angel Medical Systems, Inc.

Recalled Item: Brand Name: The Guardian System Product Name: The Guardian Model/Catalog...

The Issue: Device reaching End of Service prematurely.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vitals Monitor Recalled by Philips North America Llc Due to A...

The Issue: A software issue prevents the monitor from alarming when the high/low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Maximal Barrier Kit Recalled by Access Vascular,...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Recalled by Access Vascular, Inc Due to Specific...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vital Signs Monitor Recalled by Philips North America Llc Due...

The Issue: A software issue prevents the monitor from alarming when the high/low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: Citrine Triple Quad Mass Spectrometer Recalled by AB Sciex, LLC Due to In...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: API3200MD Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing