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. 2,877 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,877 in last 12 months

Showing 52215240 of 29,093 recalls

Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Truliant Knee System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Truliant Recalled by Exactech, Inc. Due to Exactech has received 3...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Vantage Ankle System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: AcuMatch Hip System Recalled by Exactech, Inc. Due to Exactech has received...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Equinoxe Reverse Shoulder System Recalled by Exactech, Inc. Due to...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Optetrak Knee System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Optetrak Logic Knee System Recalled by Exactech, Inc. Due to...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Medtronic Inc.

Recalled Item: Protege GPS Self-Expanding Peripheral Stent System Recalled by Medtronic...

The Issue: Seal defects could compromise the ability of the product packaging to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirTouch F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model:...

The Issue: Instructions for Use-User Deviations related to the reprocessing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit N10 Nasal Masks and User Guide Recalled by ResMed Ltd. Due to Masks...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit F30i Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit F30 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· Keystone Industries

Recalled Item: KeySplint Hard Clear - Indicated for the fabrication of orthodontic Recalled...

The Issue: Keyprint Keysplint Hard Clear 1 kg resin bottles were inadvertently packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· ROi CPS LLC

Recalled Item: Regard Dressing change kit Recalled by ROi CPS LLC Due to ROi CPS...

The Issue: ROi CPS manufactured and distributed medical convenience kits with an...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore PEGASUS (PROCESSOR Recalled by LEICA BIOSYSTEMS NUSSLOCH...

The Issue: There is an issue regarding poorly processed and/or damaged biopsy tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3 CAL2351 Recalled by Randox Laboratories Ltd. Due...

The Issue: CK Total in Calibration Serum Level 3, CAL2351, is running with a positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model:...

The Issue: Instructions for Use-User Deviations related to the reprocessing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit N20 Nasal Mask and User Guide Recalled by ResMed Ltd. Due to Masks...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing