FDADecember 6, 2017device
Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to store and position ophthalmological examination and diagnostic equipment, is to store and position for examination a device commonly known as a refractor.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Product has been found with a missing Washer, Retaining Ring, and/or Stop Screw. Recalling firm was notified by distributor that Refractor Suspension Arm fell on a patient s lower torso along with the arm housing
What to do
FDA enforcement status: Terminated
Brands named
reliance medical productsreliancereliance medical
Recall history
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