Data Foundry

Medical device recalls 2024

Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw… — Class II medical device recall Z-3093-2024

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-09-18, distributed nationwide. Potential for an incomplete seal on the packaging tray.

Recall numberZ-3093-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2024-05-07
Classified2024-09-10
Reported by FDA2024-09-18
DistributedNationwide (US)
Quantity2,860 units
Reason classespackaging
UPC / GTIN / UDI-DI10888277719415, 20888277719412
Lot numbers487233, 487315, 500686, 500687, 500963, 507070, 507116, 507420, 507423, 507424, 513684, 513691, 513692, 513998, 513999, 514002, 514004, 514006, 514205, 514206, 514332, 514337, 514343, 514540, 514542, 514631, 514633, 514634, 514873, 514874, 514875, 514876, 514877, 514878, 514879, 514880, 514881, 514882, 514883, 514884 and 163 more
Model numbersLF1937CR

Product

Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider, Nano-Coated, Compatible w/ FT10 37 cm FT10 SW Version 4.0.1.15 or lower. Item Number: LF1937CR.

Reason for recall

Potential for 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-3093-2024. 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.