FDA Device Intelligence
Home › KNIT-RITE, INC › SHORTY SOFTSOCK ®

SHORTY SOFTSOCK ®

KNIT-RITE, INC · Model 1SPSS181 · UDI-DI 00674854001591

DWLFQL
10
510(k) clearances
72
Adverse events (3 deaths)
4
Recalls
108
Facilities

Description

SHORTY SOFTSOCK LW HOLE 181RED 4.75"TOP 2.75"TOE X 7

Recalls

DateFirmReason
2014-03-19Zimmer, Inc.During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex.
2014-03-19Zimmer, Inc.During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex.
2014-03-19Zimmer, Inc.During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex.
2014-03-19Zimmer, Inc.During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex.

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.