FDA Device Intelligence
HomeMEDLINE INDUSTRIES, INC. › Medline

Medline

MEDLINE INDUSTRIES, INC. · Model NON21601 · UDI-DI 10080196749188

HMPNAB
10
510(k) clearances
10
Adverse events
4
Recalls
175
Facilities

Description

PAD,EYE,LARGE,2 1/8"X2 5/8",STERILE,LF

Recalls

DateFirmReason
2023-11-15MEDLINE INDUSTRIES, LP - NorthfieldMedline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile
2017-03-03Covidien LLCProduct sterility is compromised due to breach of sterile barrier
2017-03-03Covidien LLCProduct sterility is compromised due to breach of sterile barrier
2017-03-03Covidien LLCProduct sterility is compromised due to breach of sterile barrier

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.