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. 1,897 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,897 in last 12 months

Showing 1496114980 of 48,219 recalls

DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 90 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Ascend Laboratories LLC

Recalled Item: Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories LLC Due to...

The Issue: Presence of Foreign Tablet/Capsule

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

Class III — Low RiskOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 60 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 30 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 15 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFELX Peritoneal Dialysis Solution with 4.25% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: Sodium Chloride 0.9% Recalled by Fresenius Medical Care Holdings, Inc. Due...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 4.25% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 2.5 % Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 2.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
DrugApril 28, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Temperature Abuse: Product exposed to temperature outside specified limits.

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

Class III — Low RiskOngoing
Refund
FoodApril 28, 2021· NOW Health Group Inc.

Recalled Item: NOW 4x6 Acidophilus Recalled by NOW Health Group Inc. Due to Undeclared...

The Issue: Foreign capsules included in bottle. Undeclared ingredients.

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 28, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant II/IIs Stent Graft System: STENT GRAFT ETBF3216C145E ENDUR II...

The Issue: Incorrect stentstop assembly (18fr) was used to build the delivery system...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2021· Randox Laboratories Ltd.

Recalled Item: Randox RX Imola Analyser with ISE Recalled by Randox Laboratories Ltd. Due...

The Issue: An issue was identified where the software froze during processing of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2021· Quanta System, S.p.A.

Recalled Item: Olympus Sterile Optical Laser Fiber Recalled by Quanta System, S.p.A. Due to...

The Issue: Product sterility is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2021· Quanta System, S.p.A.

Recalled Item: Quanta System Sterile Optical Laser Fiber Recalled by Quanta System, S.p.A....

The Issue: Product sterility is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2021· Circulatory Technology Inc.

Recalled Item: The Better-Bladder (BB) Recalled by Circulatory Technology Inc. Due to The...

The Issue: The device is used as part of extracorporeal membrane oxygenation (ECMO)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2021· Quidel Corporation

Recalled Item: Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent Recalled by...

The Issue: In rare situations patients infected with high viral load of SARS CoV 2 may...

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

Class I — Serious Health HazardOngoing