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Adhesive Films

OMNIA SRL · Model 32.U0020.00 · UDI-DI 08056646508846

KGT Prescription
1
510(k) clearances
5
Adverse events
1
Recalls
28
Facilities

Description

10 Sterile Blisters of 5 Adhesive Films (20x20 cm) – 2 CROSS20 – Light Blue

Recalls

DateFirmReason
2008-03-05Kapp Surgical Instrument IncA portion of the labeled expiration date is missing. The expiration date on approximately half of the pouch labels distributed are missing the last digit of the year of expiration.

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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.