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 28181–28200 of 30,153 recalls
Recalled Item: Bracket Buccal Tube U7L DB/UL22 Roth MT HK 0/-14/0 Product Recalled by...
The Issue: Ormco Corporation is voluntarily recalling one (1) lot of Bracket Buccal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare PCA Plus II infusion pump system is designed for safe Recalled...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PCA 3 system cam be used in a wide range of clinical settings Recalled...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA 3 Recalled by Hospira Inc. Due to Screw rotation error...
The Issue: Screw rotation error occurring when the pump detects a mismatch between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare Pump Model 4200 PCA Infuser makes possible the Recalled by...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA infusion system with Hospira MedNet software allows clinicians...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA Infusion System with Hospira MedNet Software Recalled by...
The Issue: Screw rotation error occurring when the pump detects a mismatch between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version...
The Issue: It has come to the attention of MAQUET that there have been episodes of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent" irrigation tubing. Product Usage: The Torrent irrigation system...
The Issue: The firm was notified by their customers that there was a water leakage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge Group battery modules for use with Maquet SERVO-i Recalled by...
The Issue: When using the SERVO-i on battery power, in a very small number of cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Alere Cholestech LDX¿ high sensitivity C-Reactive Protein (hsCRP) Test...
The Issue: The Alere Cholestech LDX¿ hsCRP cassette (PN 12-807) may have increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a...
The Issue: Unapproved medical device
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN (TM) L-P SCREW Recalled by Smith & Nephew Inc Due to One batch of 4.5...
The Issue: One batch of 4.5 mm diameter Trigen Low-Profile Bone Screws were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Recalled by Linvatec...
The Issue: Incorrect blue/white suture was used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostics Inc. MIcroScan MICroSTREP plus Type 1...
The Issue: Customer complaint investigation confirmed the issue of false skipped wells...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIMGUARD Container Filters Recalled by Kimberly-Clark Corporation Due to...
The Issue: Some individual container filter units might contain thin areas that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS Pro meters (catalog number 05530199160)bar code scanner. Used...
The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Inform II Blood Glucose Monitoring System bar code scanner....
The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX ALT AST Test Cassette Recalled by Alere San Diego, Inc....
The Issue: The recall was initiated because Alere San Diego has an update for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...
The Issue: The recall was initiated because Carefusion has identified potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.