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.
Showing 25401–25420 of 30,153 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Artis zee and Artis zeego systems. x-ray Recalled by Siemens Medical...
The Issue: There is a potential problem with Artis zee and Artis zeego systems running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a...
The Issue: In the case of a loss of GUI display due to a Backlight Inverter PCBA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InTouch Critical Care Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker has received complaints from the field alleging instances where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALL Medical Breathing Circuit Filter Recalled by Pall Corporation Due to...
The Issue: Possible leak from the filter allowing a small of amount of air to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 It is intended to be used Recalled by Zimmer...
The Issue: Software corrections reactivating the cooperative endoscopy mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System...
The Issue: Covidien is conducting a medical device field correction for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.