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. 2,678 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,678 in last 12 months

Showing 2138121400 of 55,896 recalls

Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Randox Laboratories Ltd.

Recalled Item: Chemistry QC Premium Plus Recalled by Randox Laboratories Ltd. Due to The...

The Issue: The control target and range value for Sodium using the ISE indirect method...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· James Leckey Design Ltd

Recalled Item: Firefly Floorsitter Recalled by James Leckey Design Ltd Due to The firm...

The Issue: The firm received reports of a number of broken latches on the floorsitter.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Avid Medical, Inc.

Recalled Item: Custom procedure trays containing medical components needed to facilitate...

The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to Tests returning incorrect...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
DrugFebruary 17, 2020· Strides Pharma Science Limited

Recalled Item: Potassium Chloride Extended-Release Tablets USP Recalled by Strides Pharma...

The Issue: Failed Tablet/Capsules Specifications: Oversized tablets were found in one...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 17, 2020· Advanced Bionics, LLC

Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...

The Issue: hearing performance degradation due to body-fluid entering the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2020· Advanced Bionics, LLC

Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...

The Issue: hearing performance degradation due to body-fluid entering the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A software issue could potentially cause the stand and table movements to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A software issue could potentially cause the stand and table movements to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2020· ICU Medical, Inc.

Recalled Item: The Cogent Hemodynamic Monitoring System. Recalled by ICU Medical, Inc. Due...

The Issue: Firm identified software issues which leads to the patient ID and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2020· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS....

The Issue: Embolization device delivery system may fracture at the distal section...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 14, 2020· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: ev3 Pipeline Flex Embolization Device. For neurological endovascular use....

The Issue: Embolization device delivery system may fracture at the distal section...

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

Class I — Serious Health HazardOngoing