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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 98548

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

Open FDA event record

Event summary

Timeline bucket
February 01, 2026
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
On-X Life Technologies, Inc.

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

On-X Mitral Heart Valve with Conform-X Sewing Ring, Model: ONXMC-25/33

Z-2133-2026
Recall number
Z-2133-2026
Initiated
February 01, 2026
Classification
Class II
Status
Ongoing
Quantity
10

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.

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

Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.

Code information

UDI-DI: 00851788001303. Serial Numbers: A2013401, A2013402, A2013403, A2013404, A2013405, A2013407, A2013408, A2013409, A2013410, A2013411. Expiration: 2031Dec17

Distribution pattern

International distribution to the country of South Korea.

Field note

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