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. 1,053 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,053 in last 12 months

Showing 35301–35320 of 55,896 recalls

Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...

The Issue: There is a problem with the mating feature between the plate and screw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Medical Solutions USA, Inc

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

The Issue: Siemens is providing a new installation of the Residual Current Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Medical Solutions USA, Inc

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

The Issue: Siemens is providing a new installation of the Residual Current Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Teleflex Medical

Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...

The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...

The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Accuray Incorporated

Recalled Item: CyberKnife Robotic Radiosurgery System using software version 10.6 Recalled...

The Issue: Accuray has become aware of a potential safety issue involving unexpected...

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

Class II — Potential Health HazardOngoing
DrugNovember 22, 2016· Pfizer Inc.

Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection Recalled by Pfizer Inc....

The Issue: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month...

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

Class III — Low RiskOngoing
Refund
DrugNovember 22, 2016· Les Emballages Knowlton Inc.

Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...

The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige SI Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· Tepha Incorporated

Recalled Item: GalaSHAPE 3D Recalled by Tepha Incorporated Due to Endotoxin values from...

The Issue: Endotoxin values from testing of retains slightly exceeded the established...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: RFX Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· Oculus Innovative Sciences, Inc.

Recalled Item: Ceramax Skin Barrier Cream: NET WT 0.1 OZ (3 g Recalled by Oculus Innovative...

The Issue: Firm became aware that professional samples of Ceramax are not meeting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· Carestream Health Inc

Recalled Item: Carestream Touch Prime Recalled by Carestream Health Inc Due to Software...

The Issue: Software error; Carestream Health Inc, received a complaint stating that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige VH Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: Precision 500D Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: SFX Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· INO Therapeutics (dba Ikaria)

Recalled Item: Mallinckrodt Pharmaceuticals INOmax DSIR Plus delivery system. Model 10007....

The Issue: Mallinckrodt discovered that some devices may have been manufactured with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCN+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2016· GE Healthcare, LLC

Recalled Item: ADVANTX LCLP+ Recalled by GE Healthcare, LLC Due to GE Healthcare is...

The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...

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

Class II — Potential Health HazardOngoing