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 00889797101035, Lot Number 1737413

Quantity recalled50 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-1467-2023
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 58A221RT, bone stabilization and fixation

Where it was distributed

US Nationwide distribution.

Nationwide

Questions about this recall

Is stryker Ortholoc 3Di Fusion Plate MTP Right recalled?

Yes. Wright Medical Technology recalled stryker Ortholoc 3Di Fusion Plate MTP Right on 10 Apr 2023. The recall is Class II and its status is Ongoing. Recall number Z-1467-2023.

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 00889797101035, Lot Number 1737413

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

More recalls from Wright Medical Technology

All 78

Reported	Class	Recall	Company	Reason	Where
10 Apr 2024Device	CLASS II	stryker Infinity Resection Adjustment Block recalled	Wright Medical Technology	Other	NE, TX
12 Jul 2023Device	CLASS II	Stryker Infinity Alignment Frame Distal Sub-Assembly recalled	Wright Medical Technology	Sterility	TN
3 May 2023Device	CLASS II	stryker Ortholoc 3Di Fusion Plate MTP Right recalled	Wright Medical Technology	Other	Nationwide
8 Mar 2023Device	CLASS II	Ortholoc 3DSi Claw II 4 Hole Plate, Size recalled	Wright Medical Technology	Packaging Defects	Nationwide
8 Mar 2023Device	CLASS II	Ortholoc 3DSi Claw II 4 Hole Plate, Size recalled	Wright Medical Technology	Packaging Defects	Nationwide

Other Other Medical Devices recalls

All 13,778

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Device	CLASS II	Citric Complete Dry Citric Acid Concentrate recalled	Nipro Renal Soultions USA	Other	Nationwide
16 Sep 2026Device	CLASS I	Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS II	Halyard IV Start Kit Non-Sterile recalled by Avid Medical	Avid Medical	Sterility	Nationwide
16 Sep 2026Device	CLASS I	Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS II	AMS Convenience Kit: Dsaek Pack - RX recalled	Windstone Medical Packaging	Device Malfunction	Nationwide