FDA Device Intelligence
HomeVIVE HEALTH LLC › Vive

Vive

VIVE HEALTH LLC · Model SUP1079S · UDI-DI 00818323021981

ILG
8
510(k) clearances
2
Adverse events
3
Recalls
97
Facilities

Description

Bamboo Knee (Small, Black)

Recalls

DateFirmReason
2021-02-25Cardinal Health 200, LLCCardinal Health has determined that a manufacturing variance in a plastic film used to manufacture these products is causing the drapes and leggings to stick , which may prevent th
2021-02-25Cardinal Health 200, LLCCardinal Health has determined that a manufacturing variance in a plastic film used to manufacture these products is causing the drapes and leggings to stick , which may prevent th
2021-02-25Cardinal Health 200, LLCCardinal Health has determined that a manufacturing variance in a plastic film used to manufacture these products is causing the drapes and leggings to stick , which may prevent th

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.