CLASS II ONGOING Device recall · Reported 3 May 2023 · FDA Enforcement Report

stryker Ortholoc 3Di Fusion Plate MTP Right recalled

Wright Medical Technology is recalling stryker Ortholoc 3Di Fusion Plate MTP Right, distributed nationwide in the US. The recall was initiated on 10 Apr 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI/DI 00889797101011, Lot Number 1736809

Quantity recalled41 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1466-2023
FDA event ID: 92078
Recalling firm: Wright Medical Technology, Memphis, TN
Classification: Class II
Status: Ongoing
Recall initiated: 10 Apr 2023
FDA classified: 26 Apr 2023
Reported: 3 May 2023
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

10 Apr 2023	Recall initiated by company
26 Apr 2023	Classified by FDA	+16 days
3 May 2023	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.

Product as listed by the FDA

stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation

Where it was distributed

US Nationwide distribution.

Nationwide

Questions about this recall

Why was it recalled?

Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.

Which lots are affected?

UDI/DI 00889797101011, Lot Number 1736809

Where was it sold?

US Nationwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 92078

This product is part of a recall event; the main page for the event is stryker Ortholoc 3Di Fusion Plate MTP Right recalled.

Reported	Class	Recall	Company	Reason	Where
3 May 2023	CLASS II	stryker Ortholoc 3Di Fusion Plate MTP Right recalled	Wright Medical Technology	Other	Nationwide

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