Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6 — Class II medical device recall Z-1485-2026
Ongoing recall by Aesculap Inc, reported 2026-03-11, distributed nationwide. There is the potential for the length of the trocar shaft to be too long.
| Recall number | Z-1485-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap Inc, Center Valley, PA, United States |
| Recall initiated | 2026-01-15 |
| Classified | 2026-03-02 |
| Reported by FDA | 2026-03-11 |
| Distributed | Nationwide (US) |
| Quantity | 126 units |
| UPC / GTIN / UDI-DI | 04038653065547 |
| Serial numbers | 4592, 4595, 4596, 4598, 4601, 4606, 4607, 4608, 4612, 4616, 4618, 4619, 4620, 4621, 4623, 4657, 4659, 4661, 4662, 4667, 4670, 4673, 4674, 4688, 4689 and 101 more |
| Model numbers | FF399R |
Product
Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A
Reason for recall
There is the potential for the length of the trocar shaft to be too long.
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-1485-2026. 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.