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. 2,221 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,221 in last 12 months

Showing 36213640 of 30,153 recalls

Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aisys CS2 with Et Control. This anesthesia gas machine is Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aisys CS2. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire 7100 Recalled by Datex-Ohmeda, Inc. Due to Potential issue that may...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· LINEAGE BIOMEDICAL, INC

Recalled Item: NavaClick Syringe and Needle Recalled by LINEAGE BIOMEDICAL, INC Due to...

The Issue: Incorrect GTIN number on carton.

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2024· Intuitive Surgical, Inc.

Recalled Item: Ion Endoluminal System Recalled by Intuitive Surgical, Inc. Due to There is...

The Issue: There is a potential that the robotic system's instrument cart arm may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire 7900. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire View. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Amingo. OUS only. Recalled by Datex-Ohmeda, Inc. Due to Potential issue that...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Avance. This anesthesia gas machine is intended to provide general Recalled...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aisys. This anesthesia gas machine is intended to provide general Recalled...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Avance CS2 and Avance CS2 Pro. These anesthesia gas machines Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire 100. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2024· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...

The Issue: Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2024· Bard Peripheral Vascular Inc

Recalled Item: Guidewire 70cm x 1mm (0.038 ) These accessories Recalled by Bard Peripheral...

The Issue: Due to guidewires being manufactured incorrectly with the guidewires being...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: The VITROS XT Chemistry Products ALB-TP Slides is a single Recalled by...

The Issue: The reason for this recall is QuidelOrtho has determined that during normal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2024· Beckman Coulter Mishima K.K.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...

The Issue: Due to a software issues, after the instrument processes 250 racks...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2024· Covidien

Recalled Item: Covideien McGRATH MAC Video Laryngoscope Recalled by Covidien Due to IFU...

The Issue: IFU update to address device's battery handling information.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2024· DKK Dai-Ichi Shomei Co., Ltd.

Recalled Item: Aurora 4 Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...

The Issue: The weld on the light head frame can crack which could lead to problems such...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2024· Becton Dickinson & Co.

Recalled Item: BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics...

The Issue: There is a potential risk that the image colony count does not adequately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2024· Covidien

Recalled Item: McGrath Mac Video Laryngoscope Recalled by Covidien Due to Battery...

The Issue: Battery management system within Laryngoscope devices may deplete below the...

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

Class I — Serious Health HazardOngoing