MEDLINE convenience kits labeled as: 1) GYN LAPAROTOMY HARPER PACK-LF — Class II medical device recall Z-0527-2026
Ongoing recall by Medline Industries, LP, reported 2025-11-26, distributed nationwide. Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir
| Recall number | Z-0527-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-09-30 |
| Classified | 2025-11-14 |
| Reported by FDA | 2025-11-26 |
| Distributed | Nationwide (US) |
| Quantity | 570 kits |
| UPC / GTIN / UDI-DI | 10193489951608, 10195327107727, 10195327107734, 10195327298227, 10195327298548, 10195327299699, 10195327304287, 10195327361747, 10195327415952, 10195327454159, 10195327454166, 10195327535353, 10195327554170, 10198459082290, 40193489951609, 40195327107728, 40195327107735, 40195327298228, 40195327298549, 40195327299690, 40195327304288, 40195327361748, 40195327415953, 40195327454150, 40195327454167 and 3 more |
| Lot numbers | 23DDB824, 23DDC245, 23EBD224, 23EDA215, 23EDB911, 23FDB122, 23FDB287, 23FDC315, 23GDC100, 23GDC219, 23HBN435, 23HBW996, 23HDA180, 23HDB088, 23JDB593, 23KBE886, 23KMF190, 23LBF269, 23LBT933, 24BBE163, 24BBR389, 24BBT248, 24CBH709, 24DBO682, 24LMF192 |
| Model numbers | DYNJ0160684F, DYNJ0425778O, DYNJ27434R, DYNJ44848M, DYNJ44863Q, DYNJ44900P, DYNJ50047G, DYNJ50315F, DYNJ60554B, DYNJ67194B, DYNJ900298L, DYNJ900721C, PHS396954006G, PHS396975006F |
Product
MEDLINE convenience kits labeled as: 1) GYN LAPAROTOMY HARPER PACK-LF, REF DYNJ0160684F; 2) MAJOR LITHOTOMY PACK-LF, REF DYNJ0425778O; 3) MINOR VAGINAL #76-RF, REF DYNJ27434R; 4) ABDOMINAL HYST PACK, REF DYNJ44848M; 5) DA VINCI HYSTERECTOMY, REF DYNJ44863Q; 6) VAGINAL HYSTERECTOMY PACK, REF DYNJ44900P; 7) URO GYN, REF DYNJ50047G; 8) ISS VAG HYST PACK, REF DYNJ50315F; 9) PK MAJOR GYN ST MICHAEL C, REF DYNJ60554B; 10) VAGINAL HYSTERECTOMY PACK, REF DYNJ67194B; 11) LAVH, REF DYNJ900298L; 12) LITHOTOMY-LF, REF DYNJ900721C; 13) GP-T A H PACK-LF, REF PHS396954006G; 14) GP-VAG HYSTERECTOMY PACK-LF, REF PHS396975006F.
Reason for recall
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.
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-0527-2026. 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.