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FDA Recalls
›Device Recalls

FDA Device Recalls

Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.

Classification

All Class I Class II Class III

Status

All Ongoing Completed Terminated

Date

All time Past 30 days Past 12 months

Showing 241–242 of 242 recalls

Class IIIOngoing

Arctic Sun ArcticGel Pads - Medium, Product Code 317-07

C.R. Bard, Inc.

Label on product box contains the incorrect reference #317-09 while the shelf box label with barcode and the internal foil pouch label are correctly labeled with product code 317-07 and lot number NDAR0462.

June 2, 2017 · DeviceView details →

Class IIIOngoing

Medica ISE Module Calibrant A; 500 mL - 140 mmol/L Na+, 125 mmol/L Cl-, buffers and preservatives; For use with ISE Module; Product Usage: Calibrations of ISE Model for integrated electrolyte system analysis.

AMS Diagnostics, LLC

Lot was not functioning properly and not exhibiting the correct physical properties.

February 29, 2016 · DeviceView details →

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