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. 2,840 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,840 in last 12 months

Showing 91819200 of 30,153 recalls

Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Philips North America Llc

Recalled Item: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...

The Issue: If the system experiences an overvoltage / power surge it can cause a short...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· AMO Manufacturing USA, LLC

Recalled Item: iDesign Recalled by AMO Manufacturing USA, LLC Due to Aberrometer and...

The Issue: Aberrometer and precision laser systems are affected by a remote code...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· AMO Manufacturing USA, LLC

Recalled Item: Catalys Precision Laser System Recalled by AMO Manufacturing USA, LLC Due to...

The Issue: Aberrometer and precision laser systems are affected by a remote code...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of Recalled...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of Recalled...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2021· Boston Scientific Corporation

Recalled Item: HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of...

The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Biomeme, Inc.

Recalled Item: Biomeme SARS-CoV-2- Real Time RT-PCR Test Recalled by Biomeme, Inc. Due to...

The Issue: The current IFU specifies a shelf-life of one week after resuspension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen ceiling with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor with software VD12- angiography systems developed for Recalled...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane with software VD12-angiography systems developed for single...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor with software VD12-angiography systems developed for single...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen biplane with software VD12- angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane with software VD12-angiography systems developed for...

The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...

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

Class II — Potential Health HazardOngoing