MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider Nano-Coated… — Class II medical device recall Z-0118-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2023-10-25. Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packagin
| Recall number | Z-0118-2024 |
|---|---|
| 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 | 2023-08-03 |
| Classified | 2023-10-16 |
| Reported by FDA | 2023-10-25 |
| Quantity | 58 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10888277719439, 20888277719436 |
| Lot numbers | 498006, 498837, 498838, 499150, 499151 |
| Model numbers | LF1944CR |
Product
MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider Nano-Coated Complatible with FT10 Generator, REF LF1944CR. electrosurgical instrument
Reason for recall
Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.
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-0118-2024. 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.