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. 1,992 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,992 in last 12 months

Showing 70817100 of 48,219 recalls

DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Leader brand Lubricant Eye Drops (Propylene glycol Eye Drops 0.6%) Recalled...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: EQUATE brand Hydration PF Lubricant Eye Drops (Polyethylene glycol 400...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Rugby brand Lubricating Tears Eye Drops (Dextran 70 0.1% Recalled by Kilitch...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: CVS Health brand Lubricant Eye Drops (Propylene glycol 0.6%) Recalled by...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Leader brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Up&Up brand dry eye relief (Carboxymethylcellulose 0.5%) packaged in 0.5...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%) Recalled by Kilitch...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2023· Teva Pharmaceuticals USA, Inc

Recalled Item: Testosterone Gel Recalled by Teva Pharmaceuticals USA, Inc Due to OOS for...

The Issue: OOS for viscosity

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2023· Fagron Compounding Services

Recalled Item: Tropicamide 1% (10mg/mL) Recalled by Fagron Compounding Services Due to...

The Issue: Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the...

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 13.5-14.5-15.5. Indicated for endoscopic...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: 48IN (121.9CM) INJ LINE ROTATING ADAPT (900psi) Recalled by Smiths Medical...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: Medex 20IN (50.8CM) INJ LINE ROTATING ADAPT Recalled by Smiths Medical Asd...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: 1050 STOPCOCK LEFT ROTATOR OFF HANDLE Recalled by Smiths Medical Asd Inc Due...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 16-17-18. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: HIGH PRESSURE ROTATOR WITH MALE LUER LOCK Recalled by Smiths Medical Asd Inc...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: 6IN PRESSURE TUBING Recalled by Smiths Medical Asd Inc Due to There is a...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK Recalled by Smiths Medical Asd...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing