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Medichoice
OWENS & MINOR DISTRIBUTION, INC. · Model LAC2001A · UDI-DI 10885632114397
OVN
Prescription
0
510(k) clearances
40
Adverse events
10
Recalls
34
Facilities
Description
Tray Laceration 2 Comp Tray 2X2In 8Ply Gauze 4X4In 8Ply Gauze 18X26In Fenestrated Drape Kaycell Towel Blue 19X27In Iris Scissor Straight 4.5In Adson Tissue Forcep 4.75In 1X2 Teeth Latex-Free Sterile MediChoice
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-09 | LSL Healthcare Inc. | Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. |
| 2025-12-12 | Medline Industries, LP | Medline 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 |
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical 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 |
| 2014-06-12 | Medical Action Industries Inc | Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits. |
| 2014-06-12 | Medical Action Industries Inc | Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits. |
| 2014-06-12 | Medical Action Industries Inc | Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits. |
| 2014-06-12 | Medical Action Industries Inc | Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits. |
| 2014-06-12 | Medical Action Industries Inc | Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits. |
| 2014-06-12 | Medical Action Industries Inc | Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits. |
| 2014-06-12 | Medical Action Industries Inc | Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits. |
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Get your free API keyRead the docsData 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.