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. 2,383 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,383 in last 12 months

Showing 2454124560 of 27,462 recalls

Medical DeviceSeptember 27, 2013· Insulet Corporation

Recalled Item: OmniPod Insulin Management System Starter Kit Recalled by Insulet...

The Issue: Alcohol Prep Pads contained within the kit are not properly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2013· Olympus America Inc.

Recalled Item: TB-0545PC: THUNDERBEAT 5 mm Recalled by Olympus America Inc. Due to...

The Issue: Complaints of damage to various models of Thunderbeat Hand Instruments...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2013· S.A.E. AFIKIM

Recalled Item: Breeze C Scooter is a motorized electric scooter for elderly Recalled by...

The Issue: Breeze C Scooter, motorized 3-wheeled electric scooter for elderly people,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2013· B. Braun Medical, Inc.

Recalled Item: B. Braun Introcan Safety IV Catheter PUR 24G Recalled by B. Braun Medical,...

The Issue: One lot of Introcan Safety IV Catheters may not contain the anti-needlestick...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2013· Insulet Corporation

Recalled Item: OmniPod Insulin Management Product Demonstration Kit Recalled by Insulet...

The Issue: Alcohol Prep Pads contained within the kit are not properly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2013· Hamilton Medical, Inc.

Recalled Item: HAMILTON-C2 Ventilator: Manufactured by Hamilton Medical AG CH-7402 Bonaduz...

The Issue: Manufacturer defined limits for improperly functioning loudspeakers of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2013· Ethicon, Inc.

Recalled Item: Ethicon Stratafix Symmetric PDS Plus Knotless Tissue Control Device Ethicon...

The Issue: Ethicon Stratafix Symmetric PDS Plus Knotless Tissue Control Device has a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2013· Baxter Healthcare Corp.

Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to Incomplete foil seal on...

The Issue: Incomplete foil seal on one lot of sterile product.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2013· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 and DxH 600 Coulter Cellular Analysis Systems Recalled by...

The Issue: Beckman Coulter is initiating a recall for UniCel DxH 800 Coulter Cellular...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2013· Stryker Spine

Recalled Item: Stryker 1) XIA Torque Wrench 2) XIA 3 Torque Wrench Recalled by Stryker...

The Issue: Multiple complaints have reported that the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Soft Tissue Retractor Small Extendible Offset blade facilitates easy...

The Issue: The potential exists for the locking screw nut to break on the Soft Tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2013· Siemens Healthcare Diagnostics

Recalled Item: Siemens Chemistry Calibrator (CAL) used with the ADVIA Chemistry Direct...

The Issue: Siemens Healthcare Diagnostics is conducting a field correction for Siemens...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2013· Baxter Healthcare Corp.

Recalled Item: SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP...

The Issue: Baxter Healthcare Corporation is recalling the LCD display screen on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2013· Beckman Coulter Inc.

Recalled Item: COULTER LH 750 and LH 780 Analyzers. The COULTER LH Recalled by Beckman...

The Issue: The check valves may fail on the Coulter LH 750 Hematology Analyzer (PN...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre Recalled by Smiths...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Baylis Medical Corp *

Recalled Item: Baylis Medical TorFlex Transseptal Guiding Sheath Recalled by Baylis Medical...

The Issue: The TorFlex Transseptal Guiding Sheath Kits are being recalled due to the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Alere San Diego, Inc.

Recalled Item: Alere Triage¿ TOX Drug Screen Control 1 Product Generic Name: Recalled by...

The Issue: Alere San Diego, Inc. initiated a voluntary recall of Alere Triage TOX Drug...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs  25g Quincke Recalled by Smiths Medical...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2013· Smiths Medical ASD, Inc.

Recalled Item: Portex¿ Saddleblock Tray with Drugs 22g Quincke (Without Introducer)...

The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...

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

Class II — Potential Health HazardOngoing