Product Recalls in Nevada

Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,702 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,702 in last 12 months

Showing 44814500 of 28,334 recalls

Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...

The Issue: There is a risk of mistreatment as irradiation is not prevented when some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Qiagen Sciences LLC

Recalled Item: EZ2 Connect MDx-IVD Designed to perform automated isolation and purification...

The Issue: Insufficient welding leads to the heater cable becoming brittle and present...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Abbott GmbH

Recalled Item: ARCHITECT Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...

The Issue: Customer complaints were received regarding falsely elevated results for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· X-NAV Technologies, LLC

Recalled Item: X-Guide Handpiece Adaptor Sleeve 3 Recalled by X-NAV Technologies, LLC Due...

The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· X-NAV Technologies, LLC

Recalled Item: X-Guide Handpiece Adaptor Sleeve 1 Recalled by X-NAV Technologies, LLC Due...

The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Abbott GmbH

Recalled Item: Alinity i Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...

The Issue: Customer complaints were received regarding falsely elevated results for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· PACIFIC LASERTECH, LLC

Recalled Item: 25-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...

The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· PACIFIC LASERTECH, LLC

Recalled Item: N-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...

The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· PACIFIC LASERTECH, LLC

Recalled Item: 25-LHP-828 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...

The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...

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· 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· 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· 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· 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· 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· 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· 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· 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