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. 2,656 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,656 in last 12 months

Showing 3014130153 of 30,153 recalls

Medical DeviceMarch 27, 2007· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800 Plus Digital Recalled by GE OEC Medical Systems, Inc Due to Please...

The Issue: Please be aware that this is not a new recall. The firm has taken action;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2007· GE OEC Medical Systems, Inc

Recalled Item: UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to Please be aware...

The Issue: Please be aware that this is not a new recall. The firm has taken action;...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2007· Beevers Manufacturing & Supply, Inc.

Recalled Item: Cannulaide Recalled by Beevers Manufacturing & Supply, Inc. Due to...

The Issue: Cannulaide model CA 101 was recalled because the firm discovered this model...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2007· Philips Medical Systems (Cleveland) Inc

Recalled Item: No packaging. The device is a computed tomography scanner. Intended Recalled...

The Issue: When the Extended Display Firled ov View reconstruction is used, the CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2006· Biomet, Inc.

Recalled Item: PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile...

The Issue: Biomet is recalling Part Number PT-113950 PT Hybrid Glenoid Post, following...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2006· GE OEC Medical Systems, Inc

Recalled Item: OEC 8800 Flexview Recalled by GE OEC Medical Systems, Inc Due to Please be...

The Issue: Please be aware that this is not a new recall. The firm has taken action;...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2006· GE OEC Medical Systems, Inc

Recalled Item: The Axcess Cranial Screw (sometimes to as the Axcess Recalled by GE OEC...

The Issue: GE Healthcare is aware of a few instances where the Axcess Cranial Screw has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2006· GE OEC Medical Systems, Inc

Recalled Item: OEC InstaTrak 3500 Recalled by GE OEC Medical Systems, Inc Due to GE...

The Issue: GE Healthcare had recalled certain OEC InstaTrak 3500 Carts due to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2006· GE OEC Medical Systems, Inc

Recalled Item: InstaTrak with Multiple Dataset Navigation Recalled by GE OEC Medical...

The Issue: Please be aware that this is not a new recall. The firm has taken action;...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 6, 2006· Radiometer America Inc

Recalled Item: Qualicheck 1+ Recalled by Radiometer America Inc Due to The barcode for the...

The Issue: The barcode for the ABL77 on the insert incorrectly enters a control range...

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

Class III — Low RiskOngoing
Medical DeviceDecember 27, 2005· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT System 6/10/16/16P/40 configuration. No packaging Recalled by...

The Issue: The system has a gap that can appear between the upper and lower tilt stand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2005· JK Products & Services, Inc

Recalled Item: SUN|DASH RADIUS 252 tanning system Recalled by JK Products & Services, Inc...

The Issue: The firm has tracked a systematic failure in the door cord on the Sun|Dash...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2005· Siemens Hearing Instruments, Inc

Recalled Item: Siemens Prisma 2K Hearing Aid Product Usage: A behind the Recalled by...

The Issue: Siemens became aware of an issue where an infant or child could open the...

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

Class II — Potential Health HazardOngoing