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. 2,840 recalls have been distributed to New York in the last 12 months.
Showing 9081–9100 of 30,153 recalls
Recalled Item: SOMATOM Edge Plus-Computed tomography system Model 1026700 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge -Computed tomography system Model 10590000 Recalled...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use for all model numbers of the Medtronic Recalled by...
The Issue: There have been reports of stent migration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An...
The Issue: (1)Software (SW) versions V1.25.1 and lower may result in TDef (Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Senior Living Arial Emergency and Nurse Call Systems Recalled by Stanley...
The Issue: Systems are not alarming due to increased memory consumption.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Impacted lot may...
The Issue: Impacted lot may leak inside the ARIES instrument. Testing confirmed a leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM Recalled by Abbott Due to As a...
The Issue: As a result of a manufacturing error, one (1) lot of Ultimum Hemostasis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instavac Portable Suction Pump Recalled by Ohio Medical Corporation Due to...
The Issue: Increase in premature device failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas LiatSystem Recalled by Roche Molecular Systems, Inc. Due to Roche has...
The Issue: Roche has identified a small number of cobas Liat analyzer units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75...
The Issue: Firm is initiating a correction due to the possibility of fluid ingress....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-31...
The Issue: Firm is initiating a correction due to the possibility of fluid ingress....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi NAV Suction Instruments: 0-Degree Recalled by Acclarent, Inc. Due to...
The Issue: Suction Instruments were incorrectly calibrated so they may not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BV Pulsera with Software Release 2.3-A mobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veradius Unity with Software Release 2.1- Amobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BV Endura with Software Release 2.3- A mobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2...
The Issue: (1)Start-up problem: Intermittently at start-up of the system, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Ansel Modification Model Number:...
The Issue: Flexor Check-Flo Introducer Ansel Modification mislabeled. Products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Ansel Modification Model Number:...
The Issue: Flexor Check-Flo Introducer Ansel Modification mislabeled. Products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.