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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 89089

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

Open FDA event record

Event summary

Timeline bucket
December 03, 2021
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Wright Medical Technology 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

2 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 2

Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.

Z-0392-2022
Recall number
Z-0392-2022
Initiated
December 03, 2021
Classification
Class II
Status
Ongoing
Quantity
23 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The incorrect product is contained in the packaging.

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

The incorrect product is contained in the packaging.

Code information

Lot #1642103

Distribution pattern

Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom.

device · product 2 of 2

Stryker DARCO Screw, Locking, Ti6A14V, REF DC2825016, 2.7mm x 16mm.

Z-0393-2022
Recall number
Z-0393-2022
Initiated
December 03, 2021
Classification
Class II
Status
Ongoing
Quantity
250 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The incorrect product is contained in the packaging.

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

The incorrect product is contained in the packaging.

Code information

Lot #1643355

Distribution pattern

Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom.