MEDLINE convenience kits labeled as: 1) TOT/ GYN LITHOTOMY CDS — Class II medical device recall Z-0647-2025
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-0647-2025 |
|---|---|
| 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 | 478 units |
| UPC / GTIN / UDI-DI | 10195327173951, 10195327336110, 10195327412623, 10195327451295, 10195327470333, 10195327482114, 10195327527273, 40195327173952, 40195327336111, 40195327412624, 40195327451296, 40195327470334, 40195327482115, 40195327527274 |
| Lot numbers | 23BBG608, 23BLA272, 23BLA668, 23CLA196, 23ELB178, 23IBQ647, 23JBF512, 23JBF913, 23KBB932, 23LLA915, 24ABA205, 24ABV349, 24ABW239, 24BLA712, 24CBR704, 24CLA257, 24CLA715, 24EBP485 |
| Model numbers | CDS985431J, CDS985431K, CDS985431L, DYNJ44153G, DYNJ60924C, DYNJVB1280C, DYNJVB1280D |
Product
MEDLINE convenience kits labeled as: 1) TOT/ GYN LITHOTOMY CDS, REF CDS985431J; 2) TOT/ GYN LITHOTOMY CDS, REF CDS985431K; 3) TOT/ GYN LITHOTOMY CDS, REF CDS985431L; 4) GENERAL LITHOTOMY PACK, REF DYNJ44153G; 5) CHRISTUS AH GYN LAPAROSCOPY, REF DYNJ60924C; 6) D&C PACK, REF DYNJVB1280C; 7) D&C PACK, REF DYNJVB1280D
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-0647-2025. 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.