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. 2,748 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,748 in last 12 months

Showing 1744117460 of 30,153 recalls

Medical DeviceFebruary 7, 2018· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2018· Life Technologies Corporation

Recalled Item: Human Fetal Hemoglobin (HBF-1) FITC Conjugate Recalled by Life Technologies...

The Issue: Three lots of Human Fetal Hemoglobin FITC Conjugate are displaying high...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2018· GETINGE US SALES LLC

Recalled Item: VOLISTA StandOP Surgical Light Recalled by GETINGE US SALES LLC Due to The...

The Issue: The manufacturer received complaints indicating that the device's central...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· Hyphen BioMed

Recalled Item: ZYMUTEST HIA MonoStria qualitative screening assay intended for the global...

The Issue: Incorrect package insert indicating use of the kits with plasma, serum, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· Hyphen BioMed

Recalled Item: ZYMUTEST HIA IgGAM Recalled by Hyphen BioMed Due to Incorrect package insert...

The Issue: Incorrect package insert indicating use of the kits with plasma, serum, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· Hyphen BioMed

Recalled Item: ZYMUTEST HIA MonoStrip IgG Recalled by Hyphen BioMed Due to Incorrect...

The Issue: Incorrect package insert indicating use of the kits with plasma, serum, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear Recalled by ICU...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 14 cm (5.5") Appx 0.27 ml Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx. 0.57 ml Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 7" Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans Syringe Fill 360 Recalled by Shippert Medical Technologies Due...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 2000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 100 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 500 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 1000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 250 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Merit Medical Systems, Inc.

Recalled Item: 1mL Medallion Syringes Are used to inject fluids into Recalled by Merit...

The Issue: Supplier manufacturing defect with the syringe plunger tip.

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

Class II — Potential Health HazardOngoing