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. 2,567 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,567 in last 12 months

Showing 4690146920 of 55,896 recalls

Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Peel Away Kit Recalled by Argon Medical Devices, Inc Due to...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Argon Medical Devices, Inc

Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...

The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis or Artis zee system Product Usage: Axiom Artis Recalled by...

The Issue: There is a potential problem with the AXIOM Artis or Artis zee system in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Excelsior Medical Corp

Recalled Item: Excelsior Medical Sterile Triple Lead Tubing Set and Sterile Heavy Recalled...

The Issue: There is a potential for a leak. A molding defect in the connector that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Axcentria Pharmaceuticals, LLC

Recalled Item: Calcium Hydroxide Powder Recalled by Axcentria Pharmaceuticals, LLC Due to...

The Issue: One lot of Calcium Hydroxide Powder is being recalled because it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Humidifier Adaptor Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 101 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Adaptor Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Humidifier Adaptor 040 Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aqua 540 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the respiratory gas humidifier adaptor packaging may be creased...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak SW/EAU Sterile Recalled by Teleflex Medical Due to The seals of the...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak SW/EAU Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2014· Teleflex Medical

Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...

The Issue: The seals of the adaptor packaging may be creased which may potentially...

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

Class II — Potential Health HazardOngoing