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Barrier Supreme Eye Drape

STANDARD TEXTILE CO., INC. · Model 96801654 · UDI-DI 00634916352641

PUI
0
510(k) clearances
471
Adverse events
54
Recalls
401
Facilities

Description

Barrier Supreme Eye Drape, 22x22, 1 Ply Softweave, 1 Ply Barrier Supreme 7x7 Reinforcement Pad, 3" Round Fenestration, Concealed Hems Around Fenestration and Reinforcement Pad, Hemmed All Around, QCM on Front Bottom Right Corner

Recalls

DateFirmReason
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
2026-09-09Medline Industries, LPReports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.

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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.