Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM… — Class II medical device recall Z-1133-2026
Ongoing recall by MicroPort Orthopedics Inc., reported 2026-01-28, distributed in CA, CO, FL, GA, IL, KS, MD, MI…. Due to products not having FDA Premarket authorization to be distributed within the United States.
| Recall number | Z-1133-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MicroPort Orthopedics Inc., Arlington, TN, United States |
| Recall initiated | 2025-12-19 |
| Classified | 2026-01-20 |
| Reported by FDA | 2026-01-28 |
| Distributed | CA, CO, FL, GA, IL, KS, MD, MI, MO, TN, TX, WA, WI |
| Countries outside the US | BE, CN, DE, FR, GB, IT, JP |
| Quantity | 91 |
| UPC / GTIN / UDI-DI | 00192629320130 |
| Model numbers | HTHT0036 |
Product
Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software Version: N/A Product Description: HIPTURN FEM HEAD TRIAL 36MM REUSABLE
Reason for recall
Due to products not having FDA Premarket authorization to be distributed within the United States.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1133-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.