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. 2,100 recalls have been distributed to New York in the last 12 months.
Showing 6741–6760 of 30,153 recalls
Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...
The Issue: There is a potential that valve assemblies will not open. preventing fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo LNCS TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...
The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo LNOP TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...
The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo LNCS TC-I SpO2 Recalled by Masimo Corporation Due to TC-I tip clip...
The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo RD Set TC-I SpO2 Adult Reusable Ear Sensor Recalled by Masimo...
The Issue: TC-I tip clip sensor may produce readings outside the accuracy specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Information Center iX Recalled by Philips North America Due to...
The Issue: During extended operation of the MX40 with the PIC iX, the DHCP (Dynamic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single Use Distal Cover Model Number MAJ-2315 used with Recalled by...
The Issue: The Single Use Distal Cover MAJ-2315 may cause mucosal injury and/or become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia WT (P)180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections of...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile custom surgical procedure packs (1) 89-10529.04 Recalled by DeRoyal...
The Issue: The custom procedure packs contain light handle covers that have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile custom surgical procedure packs: (1) 89-10507.02 Recalled by DeRoyal...
The Issue: The custom procedure packs contain light handle covers that have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Coax (P) 150 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (P) 180 w/oLL Recalled by Draeger Medical, Inc. Due to...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Bag Set (N) 110 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventstar Coax 230 Recalled by Draeger Medical, Inc. Due to Glued connections...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kit Coax HEPA Recalled by Draeger Medical, Inc. Due to...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar breathing bag Set (P) 110 Recalled by Draeger Medical, Inc. Due to...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.