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. 2,673 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,673 in last 12 months

Showing 2432124340 of 30,153 recalls

Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2015· Carestream Health, Inc.

Recalled Item: CS 8100 Recalled by Carestream Health, Inc. Due to Units device head...

The Issue: Units device head descended unexpectedly

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2015· Carestream Health, Inc.

Recalled Item: CS 8100 3D Recalled by Carestream Health, Inc. Due to Units device head...

The Issue: Units device head descended unexpectedly

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2015· Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper...

The Issue: The taper adaptor is missing from the packaging, which may result in a delay...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2015· Cincinnati Sub-Zero Products Inc

Recalled Item: Cold Therapy Pad - cold water circulating pad Recalled by Cincinnati...

The Issue: Seals in the water path of the CT-99 cold therapy pad may separate during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings Recalled by...

The Issue: Stryker is recalling System 6 Aseptic Housing, due to a failed Continuous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2015· Elekta, Inc.

Recalled Item: Precise Digital Accelerator Intended to be used for radiation therapy...

The Issue: Elekta has identified a batch of securing bolts that fix the Gantry counter...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2015· GE Healthcare

Recalled Item: This correction applies to all GE Healthcare MRI systems with Recalled by GE...

The Issue: At certain sites, the MRU may not be connected to the magnet. In emergency...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 5, 2015· Arrow International Inc

Recalled Item: ARROW Epidural Needle Component (product number AN-05501). Epidural needles...

The Issue: The product labeling does not specify the 5 year shelf life of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2015· Clinical Innovations, LLC

Recalled Item: The Ebb Complete Tamponade System Recalled by Clinical Innovations, LLC Due...

The Issue: Clinical Innovations, LLC is voluntarily recalling the Ebb Complete...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2015· Natus Medical Incorporated

Recalled Item: EPWorks software used in the Xltek Protektor Stimulator Product Usage:...

The Issue: Software error occurs when using remote monitoring; if the remote user tries...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2015· Natus Medical Incorporated

Recalled Item: EPWorks software used in the Protektor 32 Product Usage: Uses Recalled by...

The Issue: Software error occurs when using remote monitoring; if the remote user tries...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo RT Therapist: The intended use of the SIEMENS branded ARTISTE Recalled...

The Issue: Combination of CTVision with syngo RT Therapist / syngo RT Oncologist...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2015· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit. The...

The Issue: Foreign material found within the kits. The foreign material, white or black...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2014· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 405 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics...

The Issue: Neonatal bilirubin (nBili) parameter may have increased variability when the...

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

Class II — Potential Health HazardOngoing