Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,185 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,185 in last 12 months

Showing 5261–5280 of 30,153 recalls

Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Optetrak Logic PS 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 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 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 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: Exactech Alteon Hip XLE Liner 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 Novation Hip 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 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 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 Vantage Mobile Bearing Tibial Inserts Recalled by Exactech, Inc....

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 Shoulder System Recalled by Exactech, Inc. Due to Exactech...

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· Beckman Coulter, Inc.

Recalled Item: Access Ultrasensitive Insulin only used on the DxI 9000 Access Recalled by...

The Issue: There is an issue with the Access Ultrasensitive Insulin assay protocol file...

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

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

Recalled Item: DxI 9000 Access Immunoassay Analyzer running software version 1.16 or prior...

The Issue: There are potential performance issues found in the DxI 9000 Access...

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· 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· 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· 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· ResMed Ltd.

Recalled Item: AirTouch 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