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Firefly Medical, Inc. recalls IVEA 500A Intended for Med-Surg patient care.
Recalled December 21, 2016 · FDA recall Z-0767-2017 · Firefly Medical
Hazard
The dowel pin could potentially slip out of its press fit, resulting in the product potentially slumping to one side which could cause the patient to stumble. · FDA Class II
Units
239
Sold at
Worldwide Distribution -- USA and Canada.
Description
The dowel pin could potentially slip out of its press fit, resulting in the product potentially slumping to one side which could cause the patient to stumble.
Product
IVEA 500A Intended for Med-Surg patient care.
Manufacturer(s)
Firefly Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →