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. 2,391 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,391 in last 12 months

Showing 2248122500 of 48,219 recalls

FoodJanuary 4, 2019· Ardent Mills, LLC

Recalled Item: HILLTOP HEARTH SELF RISE FLR 25LB and 50LB Recalled by Ardent Mills, LLC Due...

The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2019· Ardent Mills, LLC

Recalled Item: ARDENT H&R SR FLR Recalled by Ardent Mills, LLC Due to Potential Salmonella...

The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Universa Firm Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Angled Tip Ureteral Catheter Set with Bentson PTFE Wire Guide Recalled by...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Bander Ureteral Diversion Open-End Stent Set Recalled by Cook Inc. Due to...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Urethral Dilation Balloon Catheter with Open Tip Recalled by Cook Inc. Due...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: C-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Entry Set Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Sof-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Kwart Retro-Inject Ureteral Stent Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Wire Guide Recalled by Cook Inc. Due to The wire guide may be incorrectly...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Urethral Dilator Set Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Roadrunner Hydrophilic PC Wire Guide Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Bentson PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Angled Tip Ureteral Catheter Set Recalled by Cook Inc. Due to The wire guide...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Heavy Duty PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Malecot Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Pigtail Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Universa Soft Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing