FDA Device recall Z-1868-2018
RICHARD WOLF TUBE SET FOR TEM, REF 4170.801
- FDA Device
- Class II
- terminated
- Published 2018-05-23
On 2018-05-23 the FDA classified a Class II recall of RICHARD WOLF TUBE SET FOR TEM, REF 4170.801 by Richard Wolf, citing tube ends may be mixed up.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1868-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-11 |
| Published | 2018-05-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Richard Wolf |
| Distribution | n/a |
Product
RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery.
Reason
Tube ends may be mixed up.
Identifiers
| code_info | Lot numbers: 32062417, 32133317 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1868-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.