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Medline

MEDLINE INDUSTRIES, INC. · Model MDS0033340 · UDI-DI 10080196029136

EME Prescription
3
510(k) clearances
6
Adverse events
1
Recalls
86
Facilities

Description

DBD-BIOPSY PUNCH,STERILE,DISP,4MM,50EACH

Recalls

DateFirmReason
2021-03-30Omnia SRLOmnia SRL received a notification from the contract manufacturer informing them of inadequate sterilization processes which have been taking place at their contracted sterilizing f

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.