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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 95126

4 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 07, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
MEDLINE INDUSTRIES, LP - Northfield

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

4 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 4

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.

Z-3092-2024
Recall number
Z-3092-2024
Initiated
May 07, 2024
Classification
Class II
Status
Ongoing
Quantity
3,618 units

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
incomplete seal

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for an incomplete seal on the packaging tray.

Code information

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.

Distribution pattern

US Nationwide distribution.

device · product 2 of 4

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.

Z-3093-2024
Recall number
Z-3093-2024
Initiated
May 07, 2024
Classification
Class II
Status
Ongoing
Quantity
2,860 units

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
incomplete seal

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for an incomplete seal on the packaging tray.

Code information

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.

Distribution pattern

US Nationwide distribution.

device · product 3 of 4

Medline 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.

Z-3094-2024
Recall number
Z-3094-2024
Initiated
May 07, 2024
Classification
Class II
Status
Ongoing
Quantity
230 units

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
incomplete seal

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for an incomplete seal on the packaging tray.

Code information

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.

Distribution pattern

US Nationwide distribution.

device · product 4 of 4

Medline 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.

Z-3095-2024
Recall number
Z-3095-2024
Initiated
May 07, 2024
Classification
Class II
Status
Ongoing
Quantity
46 units

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
incomplete seal

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for an incomplete seal on the packaging tray.

Code information

Item Number: HARH36R. UDI/DI: 20193489081326 (case), 10193489081329 (each). Lot Numbers: 499617, 499843, 500207, 500315, 507265.

Distribution pattern

US Nationwide distribution.