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. 2,510 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,510 in last 12 months

Showing 1070110720 of 48,219 recalls

Medical DeviceSeptember 28, 2022· Covidien, LP

Recalled Item: Endo Stitch V-Loc 180 Absorbable Reload Recalled by Covidien, LP Due to...

The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Covidien, LP

Recalled Item: Endo Stitch V-Loc PBT Non-Absorbable Reload Recalled by Covidien, LP Due to...

The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Reusable Gel Pack Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· X-NAV Technologies, LLC

Recalled Item: X-Guide X-Mark Probe Tool -used for registering edentulous patients to...

The Issue: Product missing one of two welds connecting the tip to the shaft, if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health HOT AND COLD GEL PACK REUSABLE Recalled by Cardinal Health...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit Recalled by Synthes (USA)...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: SPEED 9X10X10mm Continuous Compression Implant Recalled by Synthes (USA)...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: SPEED 15X12X12mm Continuous Compression Implant Recalled by Synthes (USA)...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes Hammertoe Continuous Compression Implants Recalled by Synthes...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
DrugSeptember 26, 2022· AuroMedics Pharma LLC

Recalled Item: Acyclovir Sodium Injection Recalled by AuroMedics Pharma LLC Due to Presence...

The Issue: Presence of Particulate Matter: Customer complaint for a dark red, brown and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2022· AuroMedics Pharma LLC

Recalled Item: Tranexamic Acid Injection Recalled by AuroMedics Pharma LLC Due to Presence...

The Issue: Presence of Particulate Matter: Piece of metal found in a vial

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 23, 2022· LumiraDx

Recalled Item: LumiraDx SARS-CoV-2 Antigen (Ag) Liquid Quality Control Kit Catalog #:...

The Issue: Assigned vial lot numbers for the incorrect type of product. SARS-CoV-2 &...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 23, 2022· GAGA PRO LIGHTING EQUIPMENT CO.,

Recalled Item: GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Recalled by...

The Issue: GAGA Pro LLS systems was not in compliance with the FDA's Performance...

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

Class II — Potential Health HazardOngoing
FoodSeptember 23, 2022· The Chai Box

Recalled Item: THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles Recalled by The...

The Issue: Potential to be contaminated with Clostridium botulinum. Product was tested...

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

Class III — Low RiskOngoing
Refund