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. 2,715 recalls have been distributed to New York in the last 12 months.
Showing 18741–18760 of 30,153 recalls
Recalled Item: INVUITY(R) PhotonBlade(TM) Recalled by Invuity, Inc. Due to A small number...
The Issue: A small number of customer observations were recently received which related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRILL BIT MINI QUICK CONNECT 1.0MM Recalled by Zimmer Biomet, Inc. Due to A...
The Issue: A raw material anomaly was discovered in four lots of raw material and has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to BD initiated the...
The Issue: BD initiated the recall of Alaris PC unit model 8015 after the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Aviva II Meter - Product Usage: a. The Accu-Chek Recalled by Roche...
The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Recalled by...
The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900 Recalled by Tosoh...
The Issue: This recall has been initiated due to a potential malfunction of the photo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh¿Sorter 9tray Recalled by Tosoh Bioscience Inc Due to This recall has...
The Issue: This recall has been initiated due to a potential malfunction of the photo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 5 MHz Vascular Probe Recalled by Natus Neurology Inc Due to...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe Recalled by Natus Neurology Inc...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...
The Issue: Identification of excess plastic on the tip of the cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 3 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra 3D Revascularization Device It is indicated for used in Recalled by...
The Issue: Penumbra has identified an issue in these four lots involving a raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect diabetes management software app Recalled by Roche...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.