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. 2,659 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,659 in last 12 months

Showing 2854128560 of 55,896 recalls

Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - FSH Reagent Pack (10758750000302) 1931922...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right Recalled...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - Prolactin Reagent Pack (10758750000111)...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...

The Issue: Presence of Particulate Matter: organic and inorganic compounds detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...

The Issue: Superpotent Drug: lots out of specification for elevated sodium chloride and...

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...

The Issue: Superpotent Drug and Failed Stability Specifications: lot out of...

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Failed...

The Issue: Failed Stability Specifications: lot out of specification for elevated water...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: P400 PREM U/M 16FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: TEMP SENSE SILICONE 14FR5CC2W Recalled by COVIDIEN LLC Due to The...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: P400 PREM U/M 18FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...

The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing