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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94375

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

Open FDA event record

Event summary

Timeline bucket
March 07, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Olympus Corporation of the Americas

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

3 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 3

POWERSEAL 5 mm, 23 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic, colorectal, bariatric, vascular, thoracic, and gynecologic. Model/Catalog Number: PS-0523CJDA

Z-1699-2024
Recall number
Z-1699-2024
Initiated
March 07, 2024
Classification
Class II
Status
Ongoing
Quantity
160 units: (20 units US); (140 units OUS)

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 · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.

Code information

UDI-DI: 00821925044531 Lot number: CA182554

Distribution pattern

Worldwide distribution - US Nationwide and the countries of AU, CA, HK, KR.

device · product 2 of 3

POWERSEAL 5 mm, 37 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic, colorectal, bariatric, vascular, thoracic, and gynecologic. Model/Catalog Number: PS-0537CJDA

Z-1700-2024
Recall number
Z-1700-2024
Initiated
March 07, 2024
Classification
Class II
Status
Ongoing
Quantity
850 units: (400 units US);(450 units OUS)

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 · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.

Code information

UDI-DI: 00821925044555 Lot numbers: CA182543, CA182544, CA182546, CA182548, CA191230

Distribution pattern

Worldwide distribution - US Nationwide and the countries of AU, CA, HK, KR.

device · product 3 of 3

POWERSEAL 5 mm, 44 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic, colorectal, bariatric, vascular, thoracic, and gynecologic. Model/Catalog Number: PS-0544CJDA

Z-1701-2024
Recall number
Z-1701-2024
Initiated
March 07, 2024
Classification
Class II
Status
Ongoing
Quantity
150 units: (20 units US); (130 units OUS)

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 · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no energy would be delivered to the device resulting in delay in surgery.

Code information

UDI-DI:00821925044579 Lot Code: CA179370

Distribution pattern

Worldwide distribution - US Nationwide and the countries of AU, CA, HK, KR.