FDA Device Intelligence
Home › MIDMARK CORPORATION › Ritter

Ritter

MIDMARK CORPORATION · Model 9A51001-850 · UDI-DI 00841709116124

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

Description

The Ritter 230 Facial Pad, Sandy Retreat colored, is designed to increase stability for the head and neck during sensitive procedures.

Recalls

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

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.