FDADecember 3, 2013device
Cervical Extension Machine for Physical Therapy
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Review of DHRs revealed that HiPot, Continuity, load and friction re-testing was not completed on these devices during manufacturing.
What to do
FDA enforcement status: Terminated
Brands named
medx
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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