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 25412560 of 48,219 recalls

DrugApril 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Posterior Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Tibial Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Medtronic Neuromodulation

Recalled Item: Enhanced Verify Evaluation Handset (CFN HH90130FA) Recalled by Medtronic...

The Issue: Evaluation handsets may not be able to communicate with the neurostimulator...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Distal Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: L-Shaped Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Globus Medical, Inc.

Recalled Item: MAGEC 2 Rod Recalled by Globus Medical, Inc. Due to Devices for the affected...

The Issue: Devices for the affected lot were not assembled according to product...

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

Class II — Potential Health HazardOngoing
DrugApril 2, 2025· Amerisource Health Services LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...

The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2025· Amerisource Health Services LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...

The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2025· Amerisource Health Services LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...

The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 2, 2025· Preat Corp

Recalled Item: Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment Recalled by Preat...

The Issue: Due to manufacturing issues, abutment products were manufactured with screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2025· Getinge Disinfection Ab

Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...

The Issue: The frequency inverter is not programmed by supplier according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2025· Getinge Disinfection Ab

Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...

The Issue: The frequency inverter is not programmed by supplier according to...

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

Class II — Potential Health HazardOngoing
FoodApril 1, 2025· TONY'S CHOCOLONELY INC

Recalled Item: Tony's Chocolonely Everything Bar Recalled by TONY'S CHOCOLONELY INC Due to...

The Issue: Contains foreign objects (stones)

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 1, 2025· TONY'S CHOCOLONELY INC

Recalled Item: Tony's Chocolonely Dark Chocolate Almond Sea Salt Recalled by TONY'S...

The Issue: Contains foreign objects (stones)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 1, 2025· IBA Dosimetry GmbH

Recalled Item: myQA iON Recalled by IBA Dosimetry GmbH Due to Wrong analysis results can...

The Issue: Wrong analysis results can occur if the user creates two structures with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2025· Philips North America Llc

Recalled Item: Philips Brilliance CT Big Bore Recalled by Philips North America Llc Due to...

The Issue: Unintended motion issues related to Interventional Control that may lead to...

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

Class II — Potential Health HazardOngoing
DrugMarch 31, 2025· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Rocuronium Bromide 50 mg per 5mL (10mg per mL) Recalled by Denver Solutions,...

The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2025· Medisca Inc.

Recalled Item: Bimatoprost powder Recalled by Medisca 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 31, 2025· Denver Solutions, LLC DBA Leiters Health

Recalled Item: dexmedeTOMIDine HCl PF Recalled by Denver Solutions, LLC DBA Leiters Health...

The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.

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

Class II — Potential Health HazardOngoing
Refund