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. 2,678 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,678 in last 12 months

Showing 2146121480 of 55,896 recalls

DrugFebruary 7, 2020· American Health Packaging

Recalled Item: Desmopressin Acetate Tablets Recalled by American Health Packaging Due to...

The Issue: GMP Deviations: Product bottle may be absent of desiccant.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 7, 2020· Integra LifeSciences Corp.

Recalled Item: NeuraGen Nerve Guide Recalled by Integra LifeSciences Corp. Due to...

The Issue: Nonconforming product which was dispositioned for rejection was mistakenly...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 7, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys CA 19-9 Recalled by Roche Diagnostics Operations, Inc. Due to The...

The Issue: The firm has received an increased number of complaints concerning...

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

Class II — Potential Health HazardOngoing
DrugFebruary 7, 2020· AuroMedics Pharma LLC

Recalled Item: Amoxicillin and Clavulanate Potassium Tablets Recalled by AuroMedics Pharma...

The Issue: Presence of Foreign Substance: Customer complaint of a foreign substance...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2020· Invivo Corporation

Recalled Item: Monitor for the Functional Imaging System for Magnetic Resonance Imaging...

The Issue: Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 Recalled by...

The Issue: Due to high discordant Estradiol results which.potentially affects all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and Recalled by...

The Issue: Due to high discordant Estradiol results which.potentially affects all...

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

Class II — Potential Health HazardOngoing
DrugFebruary 5, 2020· Pfizer Inc.

Recalled Item: Caduet (amlodipine besylate/atorvastatin calcium) Tablets Recalled by Pfizer...

The Issue: Defective Container: products potentially could have been packaged in...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2020· Pfizer Inc.

Recalled Item: Caduet (amlodipine besylate/atorvastatin calcium) Tablets Recalled by Pfizer...

The Issue: Defective Container: products potentially could have been packaged in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2020· CareFusion 303, Inc.

Recalled Item: CareFusion Alaris Pump Module Recalled by CareFusion 303, Inc. Due to...

The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2020· CareFusion 303, Inc.

Recalled Item: CareFusion Alaris PCA Module Recalled by CareFusion 303, Inc. Due to 1)Error...

The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2020· CareFusion 303, Inc.

Recalled Item: CareFusion Alaris System Recalled by CareFusion 303, Inc. Due to 1)Error...

The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2020· CareFusion 303, Inc.

Recalled Item: CareFusion Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to...

The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2020· Wilson-Cook Medical Inc.

Recalled Item: HEMO-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....

The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2020· Wilson-Cook Medical Inc.

Recalled Item: HEMO-10 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....

The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2020· LivaNova USA Inc

Recalled Item: VNS Therapy Programmer Recalled by LivaNova USA Inc Due to False positive...

The Issue: False positive warning may occur after: 1) VNS Generator interrogated at 0mA...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2020· Materialise N.V.

Recalled Item: TRUMATCH Orthognathic - Full Bimaxillary Surgical Kit Recalled by...

The Issue: Custom surgical kits contain a plate different than indicated by the package...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2020· Conformis, Inc.

Recalled Item: iTotal PS Knee Replacement System Recalled by Conformis, Inc. Due to A...

The Issue: A limited number of tibial trays were labeled with an incorrect serial...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2020· Conformis, Inc.

Recalled Item: iTotal CR Knee Replacement System Recalled by Conformis, Inc. Due to A...

The Issue: A limited number of tibial trays were labeled with an incorrect serial...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2020· Radiometer Medical ApS

Recalled Item: ABL90 FLEX Analyzer Recalled by Radiometer Medical ApS Due to The firm...

The Issue: The firm received reports of occurrences where the barcode reader...

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

Class II — Potential Health HazardOngoing