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. 2,674 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,674 in last 12 months

Showing 2582125840 of 52,535 recalls

DrugSeptember 21, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Dr. Reddy's...

The Issue: Failed stability specifications - An out of specification result was...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2018· Teva Pharmaceuticals USA

Recalled Item: Clozapine Orally Disintegrating Tablets Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Disintegration Specifications: Out-of-specification disintegration...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
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
DrugSeptember 20, 2018· Pfizer Inc.

Recalled Item: Meropenem for Injection Recalled by Pfizer Inc. Due to Lack of assurance of...

The Issue: Lack of assurance of sterility: loss of container integrity.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2018· Pfizer Inc.

Recalled Item: Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle...

The Issue: CGMP Deviations; rejected product was used to manufacture final bulk lot

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 20, 2018· Lamb Weston Inc

Recalled Item: Formed Hash Brown Patties Recalled by Lamb Weston Inc Due to Hash brown...

The Issue: Hash brown product, sold under brands Brookshire's, Market Pantry,...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund