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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 91764

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

Open FDA event record

Event summary

Timeline bucket
March 06, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Maquet Cardiovascular, LLC

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

VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Model Number C-VH-3500

Z-1335-2023
Recall number
Z-1335-2023
Initiated
March 06, 2023
Classification
Class II
Status
Ongoing
Quantity
900 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Some batches of product were not sterilized to their minimum sterilization specification.

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

Some batches of product were not sterilized to their minimum sterilization specification.

Code information

UDI-DI: 00607567701250; Lot Numbers: 3000280189, 3000276183

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, China.

device · product 2 of 3

VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System, Model Number C-VH-4000

Z-1336-2023
Recall number
Z-1336-2023
Initiated
March 06, 2023
Classification
Class II
Status
Ongoing
Quantity
2300 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Some batches of product were not sterilized to their minimum sterilization specification.

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

Some batches of product were not sterilized to their minimum sterilization specification.

Code information

UDI-DI: 00607567700406; Lot Numbers: 3000278401, 3000271148, 3000268643, 3000263026, 3000274504, 3000263925

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, China.

device · product 3 of 3

VASOVIEW HEMOPRO, OUS, Endoscopic Vessel Harvesting System, Model Number C-VH-3000-W

Z-1337-2023
Recall number
Z-1337-2023
Initiated
March 06, 2023
Classification
Class II
Status
Ongoing
Quantity
235 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Some batches of product were not sterilized to their minimum sterilization specification.

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

Some batches of product were not sterilized to their minimum sterilization specification.

Code information

UDI-DI: 00607567700345; Lot Numbers: 3000274687

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, China.