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. 1,054 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,054 in last 12 months

Showing 30221–30240 of 55,896 recalls

Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
DrugJanuary 4, 2018· International Laboratories, LLC

Recalled Item: Clopidogrel Tablets Recalled by International Laboratories, LLC Due to...

The Issue: LABELING: LABEL MIX-UP. Simvastatin tablets, USP 10 mg were found in bottles...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 3, 2018· AVKARE Inc.

Recalled Item: Lovastatin Tablets USP Recalled by AVKARE Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: Low out of specification results for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 3, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Radiology CT with 4.2.0 software version. Model Recalled...

The Issue: Software issues including: Software errors that may result in Extended Field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #'...

The Issue: Software issues including: Software errors that may result in Extended Field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Zimmer Biomet, Inc.

Recalled Item: Trabecular Metal¿ Primary Hip Prosthesis Recalled by Zimmer Biomet, Inc. Due...

The Issue: Two lots of hip implants are mislabeled.

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

Class II — Potential Health HazardOngoing
FoodJanuary 3, 2018· Fieldbrook Foods Corporation

Recalled Item: Ice Cream Variety Packs containing Sandwiches Recalled by Fieldbrook Foods...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2018· Fieldbrook Foods Corporation

Recalled Item: RASPBERRY Cream Ice Cream Bars: Sundae SHOPPE Recalled by Fieldbrook Foods...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2018· Fieldbrook Foods Corporation

Recalled Item: Chocolate Covered Vanilla Ice Cream Bars packaged under the following...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2018· Fieldbrook Foods Corporation

Recalled Item: Orange Cream Ice Cream Bars sold under the following labels: Recalled by...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 3, 2018· Teleflex Medical

Recalled Item: Percuvance(R) Percutaneous Shaft 29cm Recalled by Teleflex Medical Due to...

The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Teleflex Medical

Recalled Item: Percuvance(R) Percutaneous Shaft 36cm Recalled by Teleflex Medical Due to...

The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...

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

Class II — Potential Health HazardOngoing
DrugJanuary 2, 2018· Aurobindo Pharma Ltd.

Recalled Item: Ampicillin and Sulbactam for Injection 1.5 g vial Recalled by Aurobindo...

The Issue: Presence of Particulate Matter: A confirmed customer report was received for...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 2, 2018· Roche Diagnostics Corporation

Recalled Item: Roche Acetaminophen assay 03255379160-HAcetaminophen (P) 20767174160- cobas...

The Issue: The previous version of method sheets for the Acetaminophen assay on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Thyroid Stimulating Hormone (TSH) Flex¿ reagent cartridge...

The Issue: The concentrations for biotin listed in the non-interfering substances...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Folic Acid Recalled by Siemens...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur¿ Cyclosporine Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: The concentrations for biotin listed in the non-interfering substances...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 Vitamin B12 Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable...

The Issue: An EEPROM chip error code may occur when the catheters are used with CARTO...

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

Class II — Potential Health HazardOngoing