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. 1,246 recalls have been distributed to New York in the last 12 months.
Showing 341–360 of 30,153 recalls
Recalled Item: Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Recalled...
The Issue: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. Recalled by Philips...
The Issue: It was found that the MX40 device could not reconnect to the PIC iX when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Recalled...
The Issue: Due to damage to outer tray that can potentially compromise the sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number:...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is used for the evaluation of the intrinsic coagulation pathway...
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number:...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mazor X robotic guidance system Recalled by Mazor Robotics Ltd Due to...
The Issue: Software errors that can result in incorrect surgical instrument positioning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System with Particle Therapy License (License...
The Issue: Using oncology information system that manages workflow may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LDL-Cholesterol assay is comprised of two distinct phases. In Recalled...
The Issue: Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Systems R3.0. Includes the following label descriptions and...
The Issue: Nine (9) identified software issues which may result in the following: loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.