Home › KNIT-RITE, INC › GOGO by THERAFIRM®

GOGO by THERAFIRM®

KNIT-RITE, INC · Model 24425 · UDI-DI 00721734244255

DWL FQL

510(k) clearances

Adverse events (3 deaths)

Recalls

104

Facilities

Description

GOGO TRAVEL SOCKS 3 pack- Sky Points, Berry Stripes, Black Out 15-20 MD

Recalls

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