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Lower risk Medical device recall · FDA · Published May 7, 2024

Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider Recall

Medline recalls specific models of jaw sealers due to potential incomplete packaging seals. Affected units may have packaging issues; contact Medline for details.

🇺🇸 FDA recall #Z-3093-2024Medical deviceMedline ›
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Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer

What happened, in plain English

Medline is recalling certain models of jaw sealers that may have incomplete packaging seals. This could lead to packaging issues during use, though the risk is not severe. Read more at govinfonow.com/recall/55158-medline-renewal-reprocessed-covidien-ligasure-maryland-jaw-sealer-divider-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/55158-medline-renewal-reprocessed-covidien-ligasure-maryland-jaw-sealer-divider-recall · Updated August 19, 2026 · FDA enforcement record: FDA #Z-3093-2024

Cite this page

“Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider Recall.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/55158-medline-renewal-reprocessed-covidien-ligasure-maryland-jaw-sealer-divider-recall. Based on FDA recall #Z-3093-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3093-2024%22&limit=1).

Why it’s dangerous

The packaging tray may not seal completely, potentially causing issues with the device during use. However, the hazard is not described as causing serious injury or death.

Who’s affected

Healthcare professionals using the Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider may be affected. Those with the specific model numbers listed are most at risk.

How to tell if you have this one

Check for the model number LF1937CR on the packaging. Affected units have specific lot numbers listed in the recall notice, including many numbers starting with 514000.

  • Brand
    Medline
  • Category
    Medical device
FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    US Nationwide distribution.
Recall numberProduct, codes & lotsQuantity
Z-3092-2024Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip, Sealer/Divider, Nano-Coated, Compatible w/ FT10 37cm FT10 SW Version 4.0.1.15 or lower. Item Number: LF1837CR.; Item Number: LF1837CR. UDI/DI: 20888277680392 (case), 10888277680395 (each). Lot Numbers: 487233, 487315, 487475, 487511, 499861, 499917, 500068, 500138, 500201, 500290, 500341, 500500, 500502, 500522, 500524, 500610, 500614, 500656, 500657, 507286, 507341, 507381, 507382, 507384, 507389, 507390, 507575, 513875, 514206, 514498, 514503, 514611, 514613, 514635, 514636, 514848, 514849, 514850, 514851, 514852, 514853, 514854, 514855, 514856, 515029, 515030, 515031, 515032, 515033, 515034, 515035, 515036, 515037, 515038, 515187, 515188, 515189, 515190, 515191, 515192, 515193, 515194, 515195, 515196, 515197, 515242, 515243, 515244, 515245, 515285, 515286, 515287, 515288, 515338, 515339, 515419, 515420, 515421, 515422, 515423, 515424, 515425, 515426, 515427, 515428, 515429, 515430, 515431, 515432, 515433, 515466, 515467, 515468, 515469, 515470, 515471, 515567, 515673, 515674, 515675, 515676, 515677, 515678, 515679, 515680, 515681, 515682, 515683, 515684, 515685, 515686, 515761, 515763, 515833, 515839, 515949, 515950, 515951, 516078, 516079, 516080, 516081, 516082, 516083, 516084, 516085, 516086, 516089, 516090, 516211, 516212, 516220, 516222, 516223, 516224, 516225, 516257, 516258, 516259, 516260, 516265, 516266, 516268, 516269, 516271, 516272, 516274, 516275, 516277, 516299, 516397, 516506, 516546, 516547, 516548, 516719, 516720, 516724, 516725, 516726, 516727, 516732, 516733, 516747, 516748, 516750, 516753, 516755, 516761, 516762, 516763, 516764, 516765, 516766, 516767, 516769, 516770, 516771, 516772, 516773, 516774, 516775, 516867, 516868, 516871, 516878, 516880, 517095, 517096, 517097, 517209, 517210, 517211, 517212, 517213, 517214, 517215, 517246, 517249, 517429, 517430, 517431, 517433, 517435, 517436, 517694, 517695, 517696, 517697, 517698, 517699, 517700, 517702, 517703, 517704, 517705, 517779, 517780, 517781, 517782, 517783, 517784, 517785, 517786, 517932, 518016, 518017, 518019, 518020, 518021, 518022, 518023, 518024, 518025, 518026, 518027, 518028, 518029, 518150, 518152, 518154, 518155, 518157, 518158, 518289, 518292, 518532, 518533, 518534, 518535, 518536, 518537, 518538, 518539, 518541, 518542, 518621, 518633, 518670, 518819, 518822, 518830.3,618 units
Z-3093-2024Medline 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.; 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, 518625.2,860 units
Z-3094-2024Medline ReNewal Reprocessed Covidien LigaSure Impact, Sealer/Divider, Nano-Coated, Compatible w/ FT10 18cm FT10 SW Version 4.0.1.15 or lower. Item Number: LF4418CR.; Item Number: LF4418CR. UDI/DI: 20888277680446 (case), 10888277680449 (each). Lot Numbers: 500376, 500379, 500380, 500381, 500382, 500504, 500506, 500548, 500559, 500652, 500695, 500874, 503004, 503289.230 units
Z-3095-2024Medline ReNewal Reprocessed Ethicon Harmonic ACE+7 Shears w/ Adv. Hemostasis Use Only w/GEN11 SW v2018-1 and Lower 5mm x 36cm. Item Number: HARH36R.; Item Number: HARH36R. UDI/DI: 20193489081326 (case), 10193489081329 (each). Lot Numbers: 499617, 499843, 500207, 500315, 507265.46 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the model number LF1937CR and lot numbers listed in the recall notice.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 4 months after the firm started it.

1. Firm started the recall: May 7, 202412. FDA classified it Class II: Sep 10, 202423. Published in FDA’s Enforcement Report: Sep 18, 202432024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-3093-2024 (May 7, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3093-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA