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. 1,677 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,677 in last 12 months

Showing 4608146100 of 48,219 recalls

Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: B. Braun Medical Inc. has become aware of an issue with the Outlook ES...

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

Class II — Potential Health HazardOngoing
DrugOctober 24, 2012· GlaxoSmithKline, LLC.

Recalled Item: Advair HFA (fluticasone propionate 45 mcg and salmeterol 21 mcg) Recalled by...

The Issue: Product Lacks Stability: These lots are being recalled due to the failure to...

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

Class III — Low RiskOngoing
Refund
DrugOctober 24, 2012· GlaxoSmithKline, LLC.

Recalled Item: Advair HFA (fluticasone propionate/salmeterol) Inhalation Aerosol Recalled...

The Issue: Product Lacks Stability: These lots are being recalled due to the failure to...

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

Class III — Low RiskOngoing
Refund
DrugOctober 23, 2012· Estee Lauder Inc

Recalled Item: ESTEE LAUDER DayWear Sheer Tint Release Recalled by Estee Lauder Inc Due to...

The Issue: Failed Stability Specifications: The active sunscreen ingredient, avobenzone...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 23, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem Recalled by Stryker...

The Issue: Stryker has received a report that single size 3.5 stem was packaged as size...

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

Class II — Potential Health HazardOngoing
FoodOctober 23, 2012· The Dannon Company, Inc - Discovery & Innovation Center

Recalled Item: Dannon Light & Fit Carb & Sugar Control Cultured Dairy Recalled by The...

The Issue: The recalled products may potentially contain metal fragment(s) from a...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 23, 2012· The Dannon Company, Inc - Discovery & Innovation Center

Recalled Item: Dannon Activia LIGHT Nonfat Yogurt Peach Flavor 4x4oz cups INGREDIENTS:...

The Issue: The recalled products may potentially contain metal fragment(s) from a...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 23, 2012· The Dannon Company, Inc - Discovery & Innovation Center

Recalled Item: Dannon Activia LIGHT Nonfat Yogurt Strawberry / Blueberry Flavor 12-4oz...

The Issue: The recalled products may potentially contain metal fragment(s) from a...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 23, 2012· Unified Seafood Company., Inc.

Recalled Item: Frozen Tuna Loins 3/5 Recalled by Unified Seafood Company., Inc. Due to...

The Issue: Unified Seafood Co is recalling Frozen Yellowfin Tuna Loin 3/5 due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 23, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: The Siemens Symbia T series is intended to aid in detecting Recalled by...

The Issue: There is a potential for the linear bearing car to fail allowing the ball...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: The Siemens Symbia S series is intended to aid in detecting Recalled by...

The Issue: There is a potential for the linear bearing car to fail allowing the ball...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2012· Becton Dickinson & Co.

Recalled Item: BD BBL Taxo XV Factor Strips Recalled by Becton Dickinson & Co. Due to In...

The Issue: In vitro diagnostic test kit was not manufactured according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Calibration Verification Recalled by Alere San Diego,...

The Issue: Out of range (increased) HDL Cholesterol results.

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

Class III — Low RiskOngoing
Medical DeviceOctober 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Multianalyte Control Recalled by Alere San Diego, Inc....

The Issue: Out of range (increased) HDL Cholesterol results.

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

Class III — Low RiskOngoing
DrugOctober 22, 2012· Hospira Inc.

Recalled Item: HEXTEND 6% Hetastarch in Lactated Electrolyte Injection Recalled by Hospira...

The Issue: Lack of Assurance of Sterility: There is the potential for the solution to...

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

Class II — Potential Health HazardOngoing
Refund