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. 1,074 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,074 in last 12 months

Showing 4461–4480 of 27,462 recalls

Medical DeviceMarch 1, 2024· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 Recalled by Thoratec Corp. Due to Potential for a leak...

The Issue: Potential for a leak path at the seal interface between the left ventricle...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs...

The Issue: Potential for positively biased results due to signal reduction over shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Alere San Diego, Inc.

Recalled Item: Abbott Cholestech LDX Battery Kit Recalled by Alere San Diego, Inc. Due to...

The Issue: There is a potential that the Cholestech LDX battery (an external battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Peel-Away Introducer - Intended for the percutaneous introduction of balloon...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Dilator With AQ Hydrophilic Coating - Intended to be used Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Trumpet Needle Guide ring can detach when excessive pressure is applied.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 Recalled by Thoratec Corp. Due to Potential for a leak...

The Issue: Potential for a leak path at the seal interface between the left ventricle...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion OB INSTRUMENT TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Trumpet Needle Guide ring can detach when excessive pressure is applied.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Chiba Biopsy Needle - Used for aspiration biopsy. PART Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Olympus Corporation of the Americas

Recalled Item: Olympus Triangle Tip Electrosurgical Knives- to be used with Olympus...

The Issue: Due to increase in complaints for the KD-640L and KD-645L Triangle Tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Trocar Needle - Used for dilating puncture sites or catheter Recalled by...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Yueh Centesis Disposable Catheter Needle - Intended for use in Recalled by...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Olympus Corporation of the Americas

Recalled Item: Olympus Triangle Tip Electrosurgical Knives- to be used with Olympus...

The Issue: Due to increase in complaints for the KD-640L and KD-645L Triangle Tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2024· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete Recalled...

The Issue: The reason for the recall is the pneumatic tubing used in the analytical...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix Yeast ID Panel is a self-inoculating (when used Recalled by...

The Issue: Esculin, a substrate used in other panels and normally in A16 well, was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix NMIC-306 Panel is a self-inoculating (when used with Recalled by...

The Issue: Products were found to have confirmed drug cross contamination prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2024· Covidien, LP

Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...

The Issue: The potential for trocar seal disengagement when using mesh products...

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

Class II — Potential Health HazardOngoing