FDA Device Intelligence
HomeCardinal Health 200, LLC › CARDINAL HEALTH

CARDINAL HEALTH

Cardinal Health 200, LLC · Model C-PG145I · UDI-DI 10885380052200

FER
10
510(k) clearances
86
Adverse events
1
Recalls
46
Facilities

Description

IODOFORM PACKING STRIP 1/4INX5YD ST

Recalls

DateFirmReason
2018-12-12Applied Medical Resources CorpUnintentional shifting of the tip insulation of the firm's electrosurgical probes.

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.