FDA Device Intelligence
Home › STERIS CORPORATION › NA

NA

STERIS CORPORATION · Model BF590 · UDI-DI 00724995193768

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

Description

The Shoulder Beach Chair attaches to the Cmax, STERIS 4085 General, STERIS 5085 SRT and STERIS 5085 General Surgical Tables seat section. and is used for open or arthroscopic 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.