FDA Device recall Z-1374-2023
Titan 0-Deg Scrotal 20 Cm, Catalog Number ES89202400
- FDA Device
- Class II
- ongoing
- Published 2023-04-19
On 2023-04-19 the FDA classified a Class II recall of Titan 0-Deg Scrotal 20 Cm, Catalog Number ES89202400 by Coloplast Manufacturing Us, citing XXX.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1374-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-01 |
| Published | 2023-04-19 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Coloplast Manufacturing Us |
| Distribution | US |
Product
Titan 0-Deg Scrotal 20 Cm, Catalog Number ES89202400; inflatable penile Prosthesis
Reason
XXX
Identifiers
| code_info | UDI/DI 05708932487368, Lot Numbers: 8849601, 8849600, 8849621 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1374-2023%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.