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. 2,000 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,000 in last 12 months

Showing 1186111880 of 29,093 recalls

Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 11 HOLE 197MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 11 HOLE 190MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: Biomet 8.0 Cannulated Screw Tap-Bone fixation screw Item Number: 110008467...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Neocis Inc.

Recalled Item: DRW-0742-01: Gen 2 Anterior Chairside Splint LLUR (lower left-upper right)...

The Issue: The LRUL and LLUR posterior chairside splints and LLUR anterior chairside...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. T15 LOW PROFILE CORTICAL SCREW 3.5mm x 28mm Recalled by Biomet Due...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Bound Tree Medical

Recalled Item: Curaplex Ambu King LTS-D Supraglottic Airway Kit with ET Tube Recalled by...

The Issue: Kit contained an incorrect catheter-tip syringe not compatible with the luer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 7 HOLE 140MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM 3.2MM CALIBRATED DRILL BIT Recalled...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK GUIDE SLEEVE 3.2MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. T15 Multi-Directional Locking Screw 3.5mm x 60mm Recalled by Biomet...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM 3.2MM LOCKING PEG 60MM Recalled by...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL3650 Simplexa VZV Direct - Product Usage: is intended for Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· Med Tec Inc

Recalled Item: Type S Extension For use with Varian Recalled by Med Tec Inc Due to...

The Issue: Potential for disengagement of the Varian Style Type-S Extension during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· Abbott Gmbh & Co. KG

Recalled Item: Alinity C Recalled by Abbott Gmbh & Co. KG Due to There is a potential to...

The Issue: There is a potential to generate incorrect patient results for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Biomet, Inc.

Recalled Item: Comprehensive VRS Inserter Recalled by Biomet, Inc. Due to The product is...

The Issue: The product is being recalled due to the central screw drill seizing inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Radiometer Medical ApS

Recalled Item: ABL80-FLEX-393-839 Box Label Recalled by Radiometer Medical ApS Due to...

The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing