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 541–560 of 55,896 recalls
Recalled Item: ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution. Recalled by...
The Issue: Fungal contamination of affected lot with Parengyodontium album.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) CATH LAB Recalled...
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) MEM MAXILLOFACIAL...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bengal King Jhal Chanachur food treats 12.34oz (350gm) Recalled by South...
The Issue: Contains undeclared peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2...
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: Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes...
The Issue: Six (6) identified software issues which may result in the following: system...
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: 2248 Banana Pudding Ice Cream Recalled by House Of Flavors, Inc. Due to...
The Issue: Undeclared soy lecithin
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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 ¿-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: 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 ¿-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: 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: 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: 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.