FDA Device recall Z-3092-2024

Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip, Sealer/Divider, Nano-Coated, Compatible w/ FT10 37cm FT10 SW Version 4.0.1.15 or l…

FDA Device
Class II
ongoing
Published 2024-09-18

On 2024-09-18 the FDA classified a Class II recall of Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip, Sealer/Divider, Nano-Coated, Compatible w/ FT10 37cm FT10 SW Version 4.0.1.15 or l… by Medline Industries Northfield, citing potential for an incomplete seal on the packaging tray.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-3092-2024
Classification	Class II
Status	ongoing
Initiated	2024-05-07
Published	2024-09-18
Last updated	2026-09-13 11:57 UTC
Company	Medline Industries Northfield
Distribution	US

Product

Medline 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.

Reason

Potential for an incomplete seal on the packaging tray.

Identifiers

code_info	Item Number: LF1837CR. UDI/DI: 20888277680392 (case), 10888277680395 (each). Lot Numbers: 487233, 487315, 487475, 48751… 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

code_info

Item Number: LF1837CR. UDI/DI: 20888277680392 (case), 10888277680395 (each). Lot Numbers: 487233, 487315, 487475, 48751…

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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3092-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.