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. 1,000 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,000 in last 12 months

Showing 33541–33560 of 52,535 recalls

Medical DeviceDecember 1, 2016· Merit Medical Systems, Inc.

Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...

The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-010-040 4.0MM Round Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8470-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· AtriCure, Inc.

Recalled Item: AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A...

The Issue: A complaint of the PRO2 jaw breaking prior to surgery being performed.

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

Class II — Potential Health HazardOngoing
FoodNovember 30, 2016· Dolce Dolci LLC dba Villa Dolce Gelato

Recalled Item: Strawberry Gelato Recalled by Dolce Dolci LLC dba Villa Dolce Gelato Due to...

The Issue: Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 30, 2016· Dolce Dolci LLC dba Villa Dolce Gelato

Recalled Item: Strawberry Sorbet Recalled by Dolce Dolci LLC dba Villa Dolce Gelato Due to...

The Issue: Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Pediatric Chamber Ocean Drains as follows: 2012-320 Ocean...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical 3620-100: Oasis dual chamber drain with in-line connectors...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical 16400 Express Mini 500 dry seal drain Product Recalled by...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Ocean Drains as follows: 2002-000 Ocean single drain Recalled...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Ocean Blood Recovery Drains as follows: 2050-000 Ocean...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes VA Implant Rack for the Compact Distal Radius System Recalled by...

The Issue: The screw rack plate was assembled incorrectly which could cause the screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Blood Recovery Drains as follows: 3650-100 Oasis...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Single Drain as follows: 3600-100 Oasis single Recalled...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing