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. 2,415 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,415 in last 12 months

Showing 1914119160 of 48,219 recalls

Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein CardioChek Starter Kit Recalled by Polymer Technology Systems,...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Thoratec Corp.

Recalled Item: HeartMate 3 Mobile Power Unit Recalled by Thoratec Corp. Due to Excessive...

The Issue: Excessive static electricity can potentially cause unrecoverable power loss...

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

Class II — Potential Health HazardOngoing
DrugNovember 27, 2019· Pfizer Inc.

Recalled Item: 25% Dextrose Injection Recalled by Pfizer Inc. Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Lot and/or expiration date.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3 Recalled by...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-se Fiber Optic Miller 2 Recalled by Flexicare Medical...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2 Recalled by...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-Use Fiber Optic Mac 3 Recalled by Flexicare Medical...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2019· SCA Pharmaceuticals, LLC

Recalled Item: Lidocaine HCl 2% 5 mL Recalled by SCA Pharmaceuticals, LLC Due to Foreign...

The Issue: Presence of Foreign Substance: Foreign material found inside the vial...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· Apothecus Pharmaceutical Corp.

Recalled Item: VCF Vaginal Contraceptive Foam Recalled by Apothecus Pharmaceutical Corp....

The Issue: Defective Delivery System: canister unit exhibiting propellant leakage or...

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

Class III — Low RiskOngoing
Refund
DrugNovember 25, 2019· Medisca, Inc.

Recalled Item: Estriol Recalled by Medisca, Inc. Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· AuroMedics Pharma LLC

Recalled Item: Vancomycin Hydrochloride for Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Discoloration: Product complaints of discoloration after reconstitution of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· OraLabs, Incorporated

Recalled Item: Petroleum jelly (White Petrolatum) USP 100% Recalled by OraLabs,...

The Issue: Cross contamination with other products: undeclared contaminants of phenol...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 25, 2019· Vyaire Medical

Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to The G6...

The Issue: The G6 bellavista 1000 US ventilators may experience intermittent failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2019· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE TUBE Recalled by Greiner Bio-One North America, Inc. Due to The...

The Issue: The Vacuette 3.5mL Serup Sep Clot Activator Tubes may have been damaged at...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2019· GE Healthcare, LLC

Recalled Item: Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended...

The Issue: GE Healthcare has become aware that there is a potential for a loose cable...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 25, 2019· GE Healthcare, LLC

Recalled Item: Carestation 620/650/650c A1 Product Usage: anesthesia systems are intended...

The Issue: GE Healthcare has become aware that there is a potential for a loose cable...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 25, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to During a...

The Issue: During a routine inspection of a system, a crack on the C-arm holder was...

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

Class II — Potential Health HazardOngoing
FoodNovember 22, 2019· Whole Foods Market

Recalled Item: Whole Foods Market Raspberry Cheesecake Italian Gelato 1 Pint (473mL)...

The Issue: Undeclared egg

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

Class II — Potential Health HazardOngoing
Refund