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. 2,689 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,689 in last 12 months

Showing 2182121840 of 30,153 recalls

Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Baxter Healthcare Corp.

Recalled Item: Automated peritoneal dialysis (APD) cycler Recalled by Baxter Healthcare...

The Issue: Baxter Healthcare Corporation is sending this communication to inform you of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: The two sets of wires (4 total wires) exiting from the EMI filters were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific Paraffin Type 3 For in vitro diagnostic use....

The Issue: Multiple complaints were received from customers indicating that they...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...

The Issue: Siemens found a defective part in their production line which could increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista Blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· CooperSurgical, Inc.

Recalled Item: Milex Arcing Diaphragm Size 95 Recalled by CooperSurgical, Inc. Due to The...

The Issue: The products have been identified to contain an incorrect size Diaphragm.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Biomet, Inc.

Recalled Item: Verso Shoulder Forked Retractor (Comprehensive Instrumentation 2 Prong...

The Issue: Zimmer Biomet Inc. Verso Shoulder Forked Retractor (Comprehensive...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing