FDA Device Intelligence
Home › MEDLINE INDUSTRIES, INC. › Medline

Medline

MEDLINE INDUSTRIES, INC. · Model DYNJP1060S · UDI-DI 10080196308200

KKKFYALROKKX
1
510(k) clearances
1
Adverse events
2
Recalls
4
Facilities

Description

PACK,UNIVERSAL,SPLIT,SIRUS

Recalls

DateFirmReason
2017-07-28Cardinal Health 200, LLCProduct 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.
2014-05-20Customed, IncCustomed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to 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.