MEDLINE convenience kits labeled as: 1) LAKELAND SINGLE BASIN PACK-LF — Class II medical device recall Z-0634-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-12-11, distributed nationwide. Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil wh
| Recall number | Z-0634-2025 |
|---|---|
| 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 | 2024-10-09 |
| Classified | 2024-12-05 |
| Reported by FDA | 2024-12-11 |
| Distributed | Nationwide (US) |
| Quantity | 14,388 units |
| UPC / GTIN / UDI-DI | 10195327109127, 10195327109134, 10195327118433, 10195327155728, 10195327181659, 10195327182229, 10195327201999, 10195327202613, 10195327221829, 10195327239480, 10195327273552, 10195327295905, 10195327331573, 10195327333119, 10195327349059, 10195327352523, 10195327428877, 10195327450861, 10195327450878, 10195327454630, 10195327475819, 10195327504533, 10195327515546, 10195327521226, 10195327523411 and 29 more |
| Lot numbers | 22DLA993, 22EBE400, 22EBS282, 22EDA376, 22FDA407, 22FLA375, 22ILA590, 22IMA730, 22IMG033, 22JDC142, 22JLA323, 22KBI121, 22KBI122, 22LME111, 22LMG820, 23ABN514, 23ADA553, 23AMA558, 23AMI184, 23BLA536, 23CBH097, 23CBT112, 23CBV810, 23CBV819, 23CDB848, 23CLB087, 23CME053, 23DDB147, 23DLA800, 23DMD912, 23EBB417, 23EBF888, 23EBR799, 23EBT659, 23EDA013, 23EMB339, 23FDC386, 23FLA366, 23FMG407, 23FMI052 and 41 more |
| Model numbers | DYNJ0619907I, DYNJ0619907K, DYNJ0619907L, DYNJ06966M, DYNJ0867331G, DYNJ0867555L, DYNJ24622K, DYNJ24628M, DYNJ41285B, DYNJ50123D, DYNJ54461F, DYNJ54461G, DYNJ54461I, DYNJ54801F, DYNJ54802I, DYNJ59816A, DYNJ60529D, DYNJ60812B, DYNJ60812C, DYNJ63883C, DYNJ63961D, DYNJ65808B, DYNJ68217A, DYNJ82257, DYNJ82267 and 2 more |
Product
MEDLINE convenience kits labeled as: 1) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907I; 2) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907K; 3) LKLND SNGL BASIN PK RFID-LF, REF DYNJ0619907L; 4) BASIN SET W/ RING BASIN, REF DYNJ06966M; 5) OPEN HEART C--BASIN PACK-LF, REF DYNJ0867331G; 6) TOTAL KNEE BASIN B PACK-LF, REF DYNJ0867555L; 7) ST. ANNE'S MINOR BASIN PACK, REF DYNJ24622K; 8) ST. ANNE'S MAJOR BASIN SET UP, REF DYNJ24628M; 9) MAJOR BASIN SET, REF DYNJ41285B; 10) BASIN PACK, REF DYNJ50123D; 11) MAJOR BASIN TRAY, REF DYNJ54461F; 12) MAJOR BASIN TRAY, REF DYNJ54461G; 13) MAJOR BASIN TRAY, REF DYNJ54461I; 14) TR-MINOR KIT-LF, REF DYNJ54801F; 15) TR-MAJOR KIT-LF, REF DYNJ54802I; 16) MAJOR BASIN PACK, REF DYNJ59816A; 17) SINGLE BASIN PACK ST VINCENT, REF DYNJ60529D; 18) BASIN PACK, REF DYNJ60812B; 19) BASIN PACK SH, REF DYNJ60812C; 20) PLASTIC BASIN PACK, REF DYNJ63883C; 21) MINOR PACK, REF DYNJ63961D; 22) OSC BREAST PACK, REF DYNJ65808B; 23) OSC BASIN PACK, REF DYNJ68217A; 24) DELNOR VASCULAR BASIN PACK, REF DYNJ82257; 25) DELNOR BASIN PACK, REF DYNJ82267; 26) STAZ MAJOR BASIN, REF DYNJ909785; 27) LUMBAR, REF DYNJ909923
Reason for recall
Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.
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-0634-2025. 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.