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 2762127640 of 29,093 recalls

Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS) Catalog Number: 1364E...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens CLINITEK Atlas Positive and Negative Control Strips for Urine...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...

The Issue: Boxes labeled as CIP5 may contain cartridges of AMP5.

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

Class III — Low RiskOngoing
Medical DeviceNovember 20, 2012· GE Healthcare It

Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...

The Issue: GE Healthcare is aware of a potential safety issue associated with the use...

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

Class III — Low RiskOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-221 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-322 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. SW-121 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-222 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Bunnell, Inc.

Recalled Item: Patient Circuit used with the Life Pulse High Frequency Ventilator. Recalled...

The Issue: Customer complaints received indicate the heater wire insulation can melt,...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2012· BioHorizons Implant Systems Inc

Recalled Item: Titanium Tack Starter Kit Recalled by BioHorizons Implant Systems Inc Due to...

The Issue: The cleaning instructions provided may not be sufficient to remove residual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· BioHorizons Implant Systems Inc

Recalled Item: AutoTac Delivery Handle Recalled by BioHorizons Implant Systems Inc Due to...

The Issue: The cleaning instructions provided may not be sufficient to remove residual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Zimmer, Inc.

Recalled Item: Coonrad/Morrey New Ulnar Revision Kit for Use with Non-Interchangeable...

The Issue: Zimmer is initiating a lot specific recall because affected lots could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Zimmer, Inc.

Recalled Item: COONMAD/MORREY TOTAL ELBOW ELBOW COMPONENT REPLACEMENT SET BUSHINGS & PINS...

The Issue: Zimmer is initiating a lot specific recall because affected lots could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Roche Diagnostics Operations, Inc.

Recalled Item: Roche COBAS INTEGRA 400 and 400 plus Analyzer Recalled by Roche Diagnostics...

The Issue: A software security issue with Oracles TNS-Listener component has been...

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

Class III — Low RiskOngoing
Medical DeviceNovember 19, 2012· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Intersept Custom Tubing Pack with or without coating ( Recalled by...

The Issue: Medtronic is initiating an Urgent Medical Device Customer Notification. We...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Enterprise 8000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Enterprise 9000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· Ge Healthcare It

Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...

The Issue: There is a potential for data loss associated with empty path names...

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

Class II — Potential Health HazardOngoing