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Midmark

MIDMARK CORPORATION · Model 9A739001-854 · UDI-DI 00841709123085

GBB
8
510(k) clearances
90
Adverse events (1 deaths)
1
Recalls
45
Facilities

Description

The standard articulating headrest allows you to tilt the patient's head or adjust for different procedures, helping improve access and patient comfort

Recalls

DateFirmReason
2014-11-14TransMotion Medical IncThe firm is finding that the stretcher chair controllers are moving the chairs involuntarily.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.