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Medichoice

OWENS & MINOR DISTRIBUTION, INC. · Model LAC1012 · UDI-DI 10885632114366

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

Description

Tray Laceration 2X2In 12Ply Gauze 4X4In 12Ply Gauze 18X26In Fenestrated Drape Kaycell Towel Blue 19X27In Iris Scissor Straight 4.5In Adson Tissue Forcep 4.75 1X2 Teeth Mosquito Halstead Curved 5In Webster Needle Holder Smooth 5In Latex-Free Sterile Medich

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.