Product Recalls in Maryland

Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,123 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,123 in last 12 months

Showing 4581–4600 of 29,093 recalls

Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo Full Face with Headgear Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Phantom 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious 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· SleepNet Corporation

Recalled Item: Mojo 2 Full Face Vented Mask Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for...

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 - Intended to be used for dilating puncture sites 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· 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· 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· 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· 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· 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· 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· 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-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· 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· 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: 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· 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· 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 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