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. 2,659 recalls have been distributed to New York in the last 12 months.
Showing 27141–27160 of 30,153 recalls
Recalled Item: Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649...
The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to The...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Composite Series Skull Clamp Recalled by Integra LifeSciences Corp. Due to...
The Issue: An investigation of an adverse trend of complaints for the Skull Clamp index...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Endoscope Processing System (REPS) Recalled by Steris Corporation...
The Issue: The air pipe that delivers unfiltered ambient air from the procedure room...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical MicroFuse Putty Recalled by Globus Medical, Inc. Due to The...
The Issue: The sterility of this product to a Sterility Assurance Level (SAL) of 10(-6)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Cat. 4341B Recalled by Carefusion 2200 Inc Due to Catheters included...
The Issue: Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-LIFT Extension Shims Extension shims are manufactured from grade 5...
The Issue: Fit variation among all lots of S-LIFT extension shims with corresponding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) SYMBIQ One-Channel Infuser Recalled by Hospira Inc. Due to Hospira...
The Issue: Hospira shipped the incorrect replaceable battery pack (Part No:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys...
The Issue: Based on a review of historic packaging validations, it was determined that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro System (Ysio Recalled by Siemens Medical Solutions...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captia Syphilis-G Test Kit Product Usage: This is an enzyme Recalled by...
The Issue: Trinity Biotech recalled Trinity Biotech Captia Syphilis IgG kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01 Recalled by H &...
The Issue: Medical device tubing used for endotracheal airway application may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Dispersion Aortic Perfusion Cannula with Duraflo...
The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayer brand A1CNow+ MULTI-TEST A1C SYSTEM TEST KITS (PART NUMBER...
The Issue: Test results from these lots may produce a high-bias reading (by up to 20%)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Mammo is a multi-modality Recalled by GE Healthcare It Due to There is...
The Issue: There is a potential safety issue with the 8.0.2 version software of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.