---
title: "Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider, Na... — FDA record Z-3093-2024 | Is It on Recall"
description: "Potential for an incomplete seal on the packaging tray."
url: https://isitonrecall.com/recall/fda-device-z-3093-2024-medline-renewal-reprocessed-covidien-ligasure-maryland-jaw-sealer-divider-nano-coated-compatible-w-f/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider, Nano-Coated, Compatible w/ FT10 37 cm FT10... — FDA record Z-3093-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 7, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: Potential for an incomplete seal on the packaging tray.
- **Classification**: Class II
- **Recalling firm**: MEDLINE INDUSTRIES, LP - Northfield
- **Quantity**: 2,860 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-3093-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3093-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Item Number: LF1937CR. UDI/DI: 20888277719412 (case), 10888277719415 (each). Lot Numbers: 487233, 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, 514885, 514886, 514887, 514939, 515183, 515184, 515185, 515186, 515238, 515239, 515240, 515241, 515246, 515247, 515248, 515249, 515281, 515282, 515283, 515284, 515285, 515433, 515461, 515462, 515463, 515464, 515519, 515520, 515521, 515522, 515523, 515524, 515525, 515527, 515561, 515562, 515563, 515564, 515565, 515566, 515568, 515569, 515760, 515762, 515764, 515765, 515766, 515767, 515768, 515832, 515834, 515835, 515836, 515837, 515838, 515839, 515840, 515841, 515842, 515843, 515844, 515963, 515991, 515992, 515993, 515994, 515995, 515996, 515997, 516002, 516087, 516088, 516091, 516092, 516156, 516163, 516164, 516165, 516214, 516215, 516216, 516217, 516218, 516219, 516220, 516221, 516223, 516261, 516262, 516267, 516270, 516273, 516276, 516277, 516393, 516401, 516402, 516404, 516491, 516492, 516493, 516494, 516495, 516497, 516498, 516499, 516500, 516501, 516503, 516504, 516505, 516541, 516542, 516543, 516544, 516545, 516721, 516722, 516723, 516728, 516729, 516730, 516731, 516740, 516745, 516746, 516749, 516752, 516754, 516756, 516870, 516872, 516882, 516883, 517086, 517094, 517933, 517935, 517936, 517940, 517944, 517945, 518078, 518079, 518080, 518081, 518082, 518147, 518148, 518149, 518150, 518151, 518293, 518294, 518296, 518297, 518546, 518550, 518553, 518556, 518622, 518624, 518625. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Nationwide distribution.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Sep 18, 2024
- **Recall initiation date**: May 7, 2024
- **Center classification date**: Sep 10, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3093-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MEDLINE INDUSTRIES, LP - Northfield records](https://isitonrecall.com/brand/medline-industries-lp-northfield/)
