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. 2,889 recalls have been distributed to New York in the last 12 months.
Showing 2741–2760 of 30,153 recalls
Recalled Item: BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475 Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Data Management System Version or Model: 440887 Catalog...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570 Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 Automated Microbiology System Version or Model: 443624...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm) Recalled...
The Issue: Patients implanted with synthetic cartilage implant, may experience a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used...
The Issue: Recalled lot does not meet specification and has reported incidents of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: Ti Locking Cap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR Suture Anchors. Tendon/ligament Recalled by Smith & Nephew Inc....
The Issue: Sterile barrier breach due to inadequate packaging design that could not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to Gradient coils...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to Gradient...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Artificial Urinary Sphincter Pressure Regulating Balloon 61-70 cm H2O...
The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS Artificial Urinary Sphincter Control Pump Recalled by Boston Scientific...
The Issue: Potential for mislabeled packaging in which a device labeled as a Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of...
The Issue: Bronchoscopic visualization system power supplies have defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to Gradient...
The Issue: Gradient coils for certain MR systems (see affected product list in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.