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 4680146820 of 48,219 recalls

FoodJuly 26, 2012· GH Foods CA LLC

Recalled Item: Pacific Coast brand Pizza Stuffed Mushrooms Recalled by GH Foods CA LLC Due...

The Issue: GH Foods CA received notification from Gills onions of a recall of onions...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 26, 2012· GlaxoSmithKline Inc

Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation...

The Issue: Does Not Deliver Proper Metered Dose: Potential content of albuterol per...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon Mini - 3721 (Charger). Product Usage: Eon Mini system Recalled by St....

The Issue: St. Jude Medical has informed your doctor that a number of cases have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Interface module for CDl System 100/101 Product Usage: The Interface...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-485 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Stryker Orthobiologics, Inc.

Recalled Item: Styker Orthobiologics Vita Plasma Separator Recalled by Stryker...

The Issue: When preparing plasma using VitaPrep, it was reported that a small amount of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon Mini - 3788 (IPG) Recalled by St. Jude Medical Due to As part of St....

The Issue: As part of St. Jude Medical's routine tracking and product monitoring, they...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Recalled by...

The Issue: St. Jude Medical has informed your doctor that a number of cases have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Philips Medical Systems North America Co. Phillips

Recalled Item: Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model...

The Issue: Philips determined that it is important to clarify information in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Philips Medical Systems North America Co. Phillips

Recalled Item: Philips HeartStart FRx 861304 Automated External Defibrillator Manufactured...

The Issue: Philips determined that it is important to clarify information in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-232 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Interface module for CDl System 500 Product Usage: The Interface Recalled by...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Aesculap Implant Systems LLC

Recalled Item: Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T Recalled by Aesculap...

The Issue: There is a possibility that the screw channel that holds the rod in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions...

The Issue: Decrease in onboard dilution recovery when using Multi-Diluent 1 that has...

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

Class II — Potential Health HazardOngoing
FoodJuly 25, 2012· Icrest International LLC

Recalled Item: OYSTER MEAT IQF 6/5# LBS KR PRODUCT OF KOREA Recalled by Icrest...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 25, 2012· Icrest International LLC

Recalled Item: OYSTER MEAT IQF TINY 40/8OZ PRODUCT OF KOREA Recalled by Icrest...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 25, 2012· Icrest International LLC

Recalled Item: Brand name is Yatta. OYSTERS 1/2 SHELL 144CT Recalled by Icrest...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 25, 2012· Icrest International LLC

Recalled Item: OYSTER MEAT IQF LARGE 5/4 LBS PRODUCT OF KOREA Recalled by Icrest...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

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

Class II — Potential Health HazardOngoing
Refund