RICHARD WOLF TUBE SET FOR TEM — Class II medical device recall Z-1868-2018
Terminated recall by Richard Wolf GmbH, reported 2018-05-23. Tube ends may be mixed up.
| Recall number | Z-1868-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Richard Wolf GmbH, Knittlingen, Germany |
| Recall initiated | 2018-03-11 |
| Classified | 2018-05-14 |
| Reported by FDA | 2018-05-23 |
| Terminated | 2022-03-09 |
| Quantity | 1,710 units |
| Lot numbers | 32062417, 32133317 |
| Model numbers | 4170.801 |
Product
RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery.
Reason for recall
Tube ends may be mixed up.
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-1868-2018. 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.