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 1366113680 of 48,219 recalls

FoodOctober 22, 2021· HELLOFRESH US

Recalled Item: HelloFresh Meal Kit Product Code 2-5-8-9-16-19-21-22-23-24-25 from...

The Issue: Products contain onions purchased from ProSource and associated with a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2021· HELLOFRESH US

Recalled Item: EveryPlate Meal Kit Product Codes 82-83-89-93-94-96-98 from Production Week...

The Issue: Products contain onions purchased from ProSource and associated with a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2021· HELLOFRESH US

Recalled Item: HelloFresh Meal Kit Product Code 2-4-5-8-15-19-20-22-24-AA from Production...

The Issue: Products contain onions purchased from ProSource and associated with a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2021· HELLOFRESH US

Recalled Item: EveryPlate Meal Kit Product Codes 83-84-86-89-92-94-97 from Production Week...

The Issue: Products contain onions purchased from ProSource and associated with a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2021· HELLOFRESH US

Recalled Item: EveryPlate Meal Kit Product Codes 82-83-86-88-89-91-92-94-95-96-97-99-100...

The Issue: Products contain onions purchased from ProSource and associated with a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 22, 2021· Thoratec Corp.

Recalled Item: Abbott HeartMate Touch Communication System Recalled by Thoratec Corp. Due...

The Issue: If LVAS communication system is trying to establish Bluetooth connection and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2021· Atrium Medical Corporation

Recalled Item: The Ocean Water Seal Chest Drain is a plastic Recalled by Atrium Medical...

The Issue: Inadequate/inappropriate Set-Up Instructions, which may result in delay in...

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

Class II — Potential Health HazardOngoing
FoodOctober 21, 2021· Onions 52

Recalled Item: 5# (LB) Ctn (box) Jumbo Red Onions Recalled by Onions 52 Due to Potential...

The Issue: Voluntary recall due to possible contamination with Salmonella Oranienburg...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 21, 2021· Onions 52

Recalled Item: 40# (LB) Ctn (box) Jumbo Yellow Onions Recalled by Onions 52 Due to...

The Issue: Voluntary recall due to possible contamination with Salmonella Oranienburg...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 21, 2021· Onions 52

Recalled Item: 12 count per 2 lb. mesh sacks with Recalled by Onions 52 Due to Potential...

The Issue: Voluntary recall due to possible contamination with Salmonella Oranienburg...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of Recalled...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of Recalled...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing