Medline custom medical procedure kits labeled as: 1) MEM… — Class II medical device recall Z-0786-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-01-08, distributed nationwide. Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical St
| Recall number | Z-0786-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-11-21 |
| Classified | 2024-12-30 |
| Reported by FDA | 2025-01-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA |
| Quantity | 3,903 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10193489344721, 10193489677881, 10193489750492, 10193489752199, 10193489759037, 10193489880335, 10193489890006, 10193489913187, 10195327020118, 10195327207540, 10888277503991, 10889942220083, 10889942925483, 40193489344722, 40193489677882, 40193489750493, 40193489752190, 40193489759038, 40193489880336, 40193489890007, 40193489913188, 40195327020119, 40195327207541, 40888277503992, 40889942220084 and 1 more |
| Lot numbers | 19ABB603, 19ABS779, 19ABV222, 19BKB772, 19CBN379, 19DBS122, 19DKB804, 19EBZ888, 19EBZ894, 19FBJ253, 19FBO513, 19FBQ049, 19FBX305, 19FKB661, 19GBF427, 19GKD118, 19IBR377, 19IKA148, 19JBK003, 19KDA566, 19KKB086, 19LBY431, 19SBD201, 20ABZ780, 20ADB316, 20AKB057, 20BDC412, 20BDC489, 20BKB114, 20CBD972, 20CBO773, 20CDA575, 20DBV565, 20EDC407, 20FBK295, 20FDB425, 20FKB215, 20GBI734, 20GBJ843, 20GBR819 and 81 more |
| Model numbers | DYNJ0660040R, DYNJ42833A, DYNJ42833B, DYNJ50692C, DYNJ54736B, DYNJ82735, DYNJ903144C, DYNJ905365A, DYNJ906474, DYNJ906474A, DYNJ907802, DYNJ907863, DYNJ908264 |
Product
Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, REF DYNJ0660040R; 2) FREE FLAP PACK-LF, REF DYNJ42833A; 3) FREE FLAP PACK-LF, REF DYNJ42833B; 4) TYMPANOPLASTY PACK, REF DYNJ50692C; 5) MAJOR CRANIOTOMY SAFETY, REF DYNJ54736B; 6) FREE FLAP CUSTOM PACK A, REF DYNJ82735; 7) NSR-SMR, REF DYNJ903144C; 8) KIT FACIAL MINORPLASTICS MOSES, REF DYNJ905365A; 9) SEPTOPLASTY, REF DYNJ906474; 10) SEPTOPLASTY, REF DYNJ906474A; 11) FREE FLAP, REF DYNJ907802; 12) MINOR DIEP, REF DYNJ907863; 13) MAIN FLAP, REF DYNJ908264.
Reason for recall
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0786-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.