FDA recall record

Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 recall — FDA Z-2615-2025

Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.

Class IIclassification
Z-2615-2025official record ID
Oct 1, 2025report date

Recall record at a glance

Official recordZ-2615-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmORTOMA AB
Report dateOct 1, 2025
Recall initiation dateJul 28, 2025
Quantity261 devices
LocationGoteborg, N/A, Sweden

Official product description

Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 Model Number: 2001 UDI-DI code: 07350137521019 Inserter Adapter OTD Pinnacle Straight REF 30-202 Model Number: 1001 UDI-DI code: 07350137520593 Reamer Adapter OTD REF 30-157 Model Number: 1003 UDI-DI code: 07350137520081 Inserter Adapter OTD REF 30-158 Model Number: 1004 UDI-DI code: 07350137520098 The Inserter Adapters are intended to be attached to a Cup Inserter Tool. The Cup Inserter Tool (impactor) is intended to be tracked by and navigated to orient and position the hip implant cup correctly relative to preoperative planned position and orientation.

Why the product was recalled

Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.

Distribution information

Worldwide - U.S. Nationwide distribution in the state of FL and the countries of Japan, Sweden.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.