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. 2,619 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,619 in last 12 months

Showing 3562135640 of 55,896 recalls

FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Pear & Cinnamon Preserves 10oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Strawberry Preserves 12oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Cherry Raspberry Preserves 12oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 20, 2016· Micromedics, Inc.

Recalled Item: Nordson Micromedics FibriJet Endoscopic Catheter Introducer Recalled by...

The Issue: The sterile packaging may contain small channels in the seal of the pouch,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens is providing software update version VA50A_SP3 to address the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Recalled by Merge Healthcare, Inc. Due to A product issues happens for...

The Issue: A product issues happens for RF projection images. If user measures on RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...

The Issue: Software defect:2D projection of contours in Verity. The defect causes...

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

Class II — Potential Health HazardOngoing
DrugOctober 19, 2016· Janssen Ortho L.L.C.

Recalled Item: Invokamet (canagliflozin and metformin HCl) tablets Recalled by Janssen...

The Issue: Labeling: Incorrect or Missing Package Insert - Xarelto prescribing...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 19, 2016· Greatbatch Medical

Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...

The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Ultroid Technologies, Inc.

Recalled Item: Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit...

The Issue: Products are not designed, qualified, manufactured, and/or managed under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Ultroid Technologies, Inc.

Recalled Item: Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes....

The Issue: Products are not designed, qualified, manufactured, and/or managed under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Ultroid Technologies, Inc.

Recalled Item: Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile...

The Issue: Products are not designed, qualified, manufactured, and/or managed under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Ultroid Technologies, Inc.

Recalled Item: Ultroid Sterile Disposable Probes sold individually Recalled by Ultroid...

The Issue: Products are not designed, qualified, manufactured, and/or managed under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Beckman Coulter Inc.

Recalled Item: AQUIOS Lyse Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the AQUIOS Lyse Reagent Kit because it may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: A problem can occur with the small light marker windows, used for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 19-9 Assay (50 test kit)-for use Recalled by Siemens...

The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...

The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: A problem can occur with the small light marker windows, used for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS system Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Hardware issue that may expose the User to a potential risk for serious...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash system Recalled by Siemens Medical Solutions USA,...

The Issue: Hardware issue that may expose the user to a potential risk for serious...

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

Class II — Potential Health HazardOngoing