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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 81430

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
June 19, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Stryker Sustainability Solutions

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

1 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 1

Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars12x100mm - Product Usage: Physical Product Description: The Reprocessed Blunt Tip Trocar consists of a radiolucent cannula and obturator sized 12mm in diameter (refer to Figure 1). The Reprocessed Blunt Tip Trocar has an obturator that has a blunt plastic tip that gently moves aside any internal viscera that may be adjacent to the abdominal or thoracic wall. The trocar cannula consists of two seals, an outer integrated removable self-adjusting seal that may accommodate instruments ranging from 5mm to 12mm in diameter, and an internal seal. These seals minimize gas leakage when instruments are inserted or withdrawn through the seal. The stopcock valve provides attachment for gas insufflation and desufflation. The stability plug component, is specific only to the H12LP catalog number. The stability plug (adjustable plug) is placed on the outside of the trocar sleeve (cannula). The stability plug provides suture clips (suture anchors), which can be used to suture the Trocar sleeve in place. Intended Use: Reprocessed Endoscopic Trocars are indicated for use to establish a port of entry for endoscopic instruments in patients requiring minimally invasive surgical procedures. Physical Product Description: The Reprocessed Blunt Tip Trocar consists of a radiolucent cannula and obturator sized 12mm in diameter (refer to Figure 1). The Reprocessed Blunt Tip Trocar has an obturator that has a blunt plastic tip that gently moves aside any internal viscera that may be adjacent to the abdominal or thoracic wall. The trocar cannula consists of two seals, an outer integrated removable self-adjusting seal that may accommodate instruments ranging from 5mm to 12mm in diameter, and an internal seal. These seals minimize gas leakage when instruments are inserted or withdrawn through the seal. The stopcock valve provides attachment for gas insufflation and desufflation. The stability plug component, is specific only to the H12LP catalog number. The stability plug (adjustable plug) is placed on the outside of the trocar sleeve (cannula). The stability plug provides suture clips (suture anchors), which can be used to suture the Trocar sleeve in place. Intended Use: Reprocessed Endoscopic Trocars are indicated for use to establish a port of entry for endoscopic instruments in patients requiring minimally invasive surgical procedures.

Z-0498-2019
Recall number
Z-0498-2019
Initiated
June 19, 2018
Classification
Class II
Status
Terminated
Quantity
4848

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Through investigation, it was determined that H12LP Trocars in scope of a previous H12LP recall were distributed to facilities within the distribution chain following the recall execution activities initially performed by distributor.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

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Inspect official wording and provenance

Reason for recall

Through investigation, it was determined that H12LP Trocars in scope of a previous H12LP recall were distributed to facilities within the distribution chain following the recall execution activities initially performed by distributor.

Code information

Lot Number 3727435 3732833 3732851 3752003 3762495 3762972 3765649 3783776 3775681 3779516 3782202 3784430 3786146 3794419 3803918 3810037 3811778 3809891 3821740 3829338 3833206 3834196 3853141 3854774 3861804 3863303 3870240 3873578 3881364 3886277 3866398 3890070 3890089 3880942 3894678 3896022 4113667 4118604 4133825 3849330 4138769 4147801 4154685 4158429 4170275 4173170 4187693 4198853 4202332 4235633 4245630 4274018 4282444 4386368 4515596 4459232 4458288 4466644 4467337 4466103 4473956 4474932 4476349 4477829 4479578 4512285 4513266 4530457 4533116 4548738 4551779 4557026 4566912 4572487 4571871 4574911 4576443 4576086 4577407 4581177 4580431 4583936 4589373 4593587 4603588 4597997 4602957 4598476 4607573 4608496 4608514 4615536 4609747 4610175 4610894 4611167 4611179 4612670 4613359 4614603 4618135 4615246 4616746 4659568 4659478 4660191 4671055 4662392 4663276 4664364 4668273 4669208 4672293 4670712 4667846 4668260 4668287 4670139 4674512 4674857 4074165 4672065 4680853 4681245 4683268 4686942 4688031 4688326 4688887 4688894 4690786 4695707 4704437 4698746

Distribution pattern

US nationwide distribution in the states of OK, GA, NJ, TX, IA, CO, TX, CA, LA, PA, VA, MD, WA, and IL. OUS: None.