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Medichoice

OWENS & MINOR DISTRIBUTION, INC. · Model LAC1010 · UDI-DI 10885632114342

OVN
0
510(k) clearances
40
Adverse events
10
Recalls
34
Facilities

Description

Tray Laceration 4X4 In 12-Ply Gauze 17X19IN Drape Blue Linen Operating Room Towel 18X26IN Fenestrated Operating Room Towel Iris Scissor Straight 4.5In Adson Tissue Forcep 4.75In 1X2 Teeth Adson Serrated Forcep 4.75In Mosquito Halstead Curved 5In Webster N

Recalls

DateFirmReason
2026-03-09LSL Healthcare Inc.Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
2025-12-12Medline Industries, LPMedline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the via
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma
2014-06-12Medical Action Industries IncSome of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12Medical Action Industries IncSome of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12Medical Action Industries IncSome of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12Medical Action Industries IncSome of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12Medical Action Industries IncSome of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12Medical Action Industries IncSome of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
2014-06-12Medical Action Industries IncSome of the sterile kits may have incomplete seals which might compromise the sterility of the kits.

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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.