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OR Specific

OR SPECIFIC, INC. · Model 418-S · UDI-DI 00841027103004

PUI
0
510(k) clearances
471
Adverse events
54
Recalls
398
Facilities

Description

Drape, Standard, For 4' Big Case Back Table Model 427 Series. Case of 10. Sterile- Each

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.