FDA Device Intelligence
HomeO&M HALYARD, INC. › Halyard

Halyard

O&M HALYARD, INC. · Model 54800 · UDI-DI 20680651548003

NZD
1
510(k) clearances
3
Adverse events
2
Recalls
61
Facilities

Description

HALYARD* O.R. Table/Stretcher Strap, 3 in. x 30 in. / 8 cm x 76 cm

Recalls

DateFirmReason
2016-03-10Ferno-Washington IncOn March 9, 2016, the firm was contacted regarding the possibility of incorrect labeling on the outside poly- bag of the traction splint straps. The firm investigated and determine
2016-03-10Ferno-Washington IncOn March 9, 2016, the firm was contacted regarding the possibility of incorrect labeling on the outside poly- bag of the traction splint straps. The firm investigated and determin

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.