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. 2,703 recalls have been distributed to New York in the last 12 months.
Showing 21201–21220 of 30,153 recalls
Recalled Item: 5195GM Recalled by Lifeline First Aid LLC Due to Cadillac First Aid Kit is...
The Issue: Cadillac First Aid Kit is recalled because it contains the CPR Shield with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saw Sagittal Catalog Number: ES 300 Recalled by Medtronic Sofamor Danek Usa,...
The Issue: Medtronic Powered Surgical Solutions testing of the Sagittal Saw Rocker Arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19...
The Issue: A patient weight can be populated incorrectly under certain conditions when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or...
The Issue: Premature bucket failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Trabecular Metal Tibia Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Zimmer Inc. is initiating a recall of specific Persona" Trabecular Metal"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 3 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Pump RF Patient Cassette Recalled by Medical Vision Ab Due to...
The Issue: Sterility of device may be compromised due to sterile package breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piccolo Composite Tibia and Femoral Nailing Systems - Ball Tip Recalled by...
The Issue: Firm received complaints where the Piccolo Composite Ball Tip Guide Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TS Series Depth Gauge for Integra Ti6 Internal Fixation System Recalled by...
The Issue: As a result of an internal investigation of a non-conformance it has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse PACS software version 4.4.000 Recalled by Fujifilm Medical...
The Issue: Synapse cannot display image files, DICOM SR files, and/or Annotation files....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Revolution CT The system is intended for head Recalled by GE Healthcare,...
The Issue: GEHC has become aware of a potential safety issue in the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products AFP Reagent Pack Recalled by ORTHO-CLINICAL...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed that specific lots of VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...
The Issue: The device was found to have bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MSK 1.5T Extreme MR Scanner Recalled by GE Healthcare, LLC Due to The gas...
The Issue: The gas venting may not occur properly. A site reported a magnet quenching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima 1.5T MR430s MR Scanner Recalled by GE Healthcare, LLC Due to The gas...
The Issue: The gas venting may not occur properly. A site reported a magnet quenching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.