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. 2,330 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,330 in last 12 months

Showing 3830138320 of 48,219 recalls

DrugDecember 19, 2014· Bethel Nutritional Consulting, Inc

Recalled Item: B-Lipo Recalled by Bethel Nutritional Consulting, Inc Due to Marketed...

The Issue: Marketed without an Approved NDA/ANDA; found to contain Lorcaserin, a...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 18, 2014· Reily Foods Co.

Recalled Item: WICK FOWLER'S FAMOUS TEXAS STYLE 2-ALARM Chili Kit Recalled by Reily Foods...

The Issue: Kits contain peanut and almond allergens that are not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2014· Reily Foods Co.

Recalled Item: CARROLL SHELBY'S ORIGINAL TEXAS BRAND CHILI KIT Recalled by Reily Foods Co....

The Issue: Kits contain peanut and almond allergens that are not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2014· Reily Foods Co.

Recalled Item: CARROLL SHELBY'S ORIGINAL TEXAS BRAND WHITE CHICKEN CHILI KIT Recalled by...

The Issue: Kits contain peanut and almond allergens that are not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2014· Reily Foods Co.

Recalled Item: WICK FOWLER'S TEXAS STYLE FALSE ALARM Mild Chili Kit Recalled by Reily Foods...

The Issue: Kits contain peanut and almond allergens that are not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 18, 2014· Sysmex Corporation

Recalled Item: The XN-Series modules (XN-10 Recalled by Sysmex Corporation Due to There is...

The Issue: There is a potential for elevated hemoglobin (Hgb) and impedance platelet...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer Recalled...

The Issue: Chemical component of the F3 Fluid pack and environmental bacterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2014· Ziemer Usa Inc

Recalled Item: Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform...

The Issue: The devices were not shipped with the Starter Kits.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2014· Spinal Elements, Inc

Recalled Item: Ti-Bond Marketing Literature/Labeling Recalled by Spinal Elements, Inc Due...

The Issue: Spinal Elements is recalling the Ti-Bond related brochures that includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2014· St Jude Medical Cardiac Rhythm Management Division

Recalled Item: Merlin@home RF Remote Monitoring Transmitter Recalled by St Jude Medical...

The Issue: Transmitter may initiate a software reset resulting in backup operation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: Metasul Femoral Head - A modular head component is used Recalled by Zimmer...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: CoCr Femoral Head - A modular head component is used Recalled by Zimmer Gmbh...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Aesculap, Inc.

Recalled Item: Miethke Shunt System accessories Product Usage: - The Miethke Shunt Recalled...

The Issue: Some Miethke Shunt System accessories may have an incorrect MR safety symbol...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB)...

The Issue: Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: CoCr Femoral Head - indicated for hip arthroplasty for noncemented Recalled...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: Biolox Delta Femoral Head - The BIOLOX delta Ceramic Femoral Recalled by...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm Recalled by Stryker...

The Issue: Potential for implant damage, implant cracking off/breaking intra-operatively.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants...

The Issue: Potential for implant deformation, implant mechanical stability too low,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block...

The Issue: Potential for implant deformation, implant mechanical stability too low,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: Metasul Femoral Head - indicated for total hip arthroplasty for Recalled by...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing