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. 1,053 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,053 in last 12 months

Showing 9381–9400 of 48,219 recalls

DrugMarch 20, 2023· RemedyRepack Inc.

Recalled Item: Rosuvastatin 10mg tablets Recalled by RemedyRepack Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2023· RemedyRepack Inc.

Recalled Item: Atorvastatin 20 mg tablets Recalled by RemedyRepack Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2023· RemedyRepack Inc.

Recalled Item: Tadalafil 5 mg tablets Recalled by RemedyRepack Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2023· RemedyRepack Inc.

Recalled Item: Ropinirole 2mg tablets Recalled by RemedyRepack Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2023· RemedyRepack Inc.

Recalled Item: Ropinirole 0.5 mg tablets Recalled by RemedyRepack Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2023· RemedyRepack Inc.

Recalled Item: Rosuvastatin 5mg tablets Recalled by RemedyRepack Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2023· Amerisource Health Services LLC

Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations: recalling drug products following an FDA inspection.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2023· Ascend Laboratories, LLC

Recalled Item: Aripiprazole Tablets Recalled by Ascend Laboratories, LLC Due to Out of...

The Issue: Out of specification (OOS) for Spectroscopic Identification test by IR.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2023· Amerisource Health Services LLC

Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations: recalling drug products following an FDA inspection.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 17, 2023· Perrigo Nutritionals

Recalled Item: Gerber GoodStart SoothePro Infant Formula with Iron. Milk Based Powder....

The Issue: Infant Formula has the potential to be contaminated with Cronobacter spp.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 17, 2023· Amerisource Health Services LLC

Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations: recalling drug products following an FDA inspection.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 17, 2023· Beaver Visitec International, Inc.

Recalled Item: CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery....

The Issue: Device suddenly and forcefully disassembled after cryotherapy, potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Steris Corporation

Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...

The Issue: Light handle covers may separate from the light handle (detach and fall off)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Steris Corporation

Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...

The Issue: Light handle covers may separate from the light handle (detach and fall off)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Medtronic Neuromodulation

Recalled Item: Medtronic SenSight Extension Tunneler Kit Recalled by Medtronic...

The Issue: Medtronic has received reports of SenSight Extension Tunneler kits that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Philips North America Llc

Recalled Item: Spectral CT 7500 Computed Tomography X-Ray System Recalled by Philips North...

The Issue: Pressing the Unload Pedal of the foot switch to perform the unload function...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2023· SPINEART SA

Recalled Item: JULIET Ti LL Recalled by SPINEART SA Due to JULIET Lateral Lumbar Ti-Life...

The Issue: JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Cortisol 50T (Material Number 10994924) Recalled by Siemens...

The Issue: There is a negative bias with urine patient samples and urine cortisol...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Cortisol 50T (Material Number 10995538) Recalled by Siemens...

The Issue: There is a negative bias with urine patient samples and urine cortisol...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2023· Ellex Medical Pty Ltd.

Recalled Item: Integre Pro Yellow LP561 Recalled by Ellex Medical Pty Ltd. Due to When...

The Issue: When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a...

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

Class II — Potential Health HazardOngoing