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. 2,800 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,800 in last 12 months

Showing 1536115380 of 29,093 recalls

Medical DeviceSeptember 24, 2018· Becton Dickinson & Co.

Recalled Item: BD Max Instrument Recalled by Becton Dickinson & Co. Due to A trend for...

The Issue: A trend for false positive Candida glabrata results has been confirmed. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Becton Dickinson & Co.

Recalled Item: BD Max Instrument Reader Spare Part Recalled by Becton Dickinson & Co. Due...

The Issue: A trend for false positive Candida glabrata results has been confirmed. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Roche Diagnostics Corporation

Recalled Item: Roche Diagnostics URISYS 1100 Urine Analyzer Part Number: 03617556001...

The Issue: Limits of Detection (LoD) for protein, nitrite, leukocytes, and erythrocytes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL AMT COXA VARA NECK SEGMENT (KLA) Pro. Code L20432 Recalled by DePuy...

The Issue: There is the potential for debris/material to be found behind the O-rings in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD) Recalled by DePuy...

The Issue: There is the potential for debris/material to be found behind the O-rings in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO) Recalled by DePuy Orthopaedics,...

The Issue: There is the potential for debris/material to be found behind the O-rings in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· Arrow International Inc

Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...

The Issue: The products labeling contains inconsistencies. In certain instances, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· Zimmer Biomet, Inc.

Recalled Item: StageOne Hip Recalled by Zimmer Biomet, Inc. Due to There is a potential for...

The Issue: There is a potential for comingling of the 43MM and 51 MM molds

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4.5 Recalled by RAYSEARCH LABORATORIES AB Due to Robust...

The Issue: Robust optimization for plans using beam set + background dose is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· Becton Dickinson & Co.

Recalled Item: BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station Recalled by...

The Issue: The device may not function at the lower end (<15 deg. C) of the labeled...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

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

Class I — Serious Health HazardOngoing