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. 2,573 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,573 in last 12 months

Showing 27612780 of 27,462 recalls

Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil Recalled by...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Non coated 70 mm Recalled by...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil Recalled by...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CARROLLTON HIP FX Convenience kit used for surgical procedures Recalled by...

The Issue: Products within a Medline pack may be impacted by a packaging error in which...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Recalled by Stryker...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button Recalled...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ARTHROSCOPY Convenience kit used for surgical procedures Recalled by MEDLINE...

The Issue: Products within a Medline pack may be impacted by a packaging error in which...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2024· Getinge Usa Sales Inc

Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...

The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...

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

Class II — Potential Health HazardOngoing