FDA Device recall Z-0923-2025
8MM, Tenaculum Forceps REF 470207 Instrument used with the da Vinci X/Xi Surgical Systems in a wide variety of procedures to perform a vari…
- FDA Device
- Class II
- ongoing
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of 8MM, Tenaculum Forceps REF 470207 Instrument used with the da Vinci X/Xi Surgical Systems in a wide variety of procedures to perform a vari… by Intuitive Surgical, citing due to an increase in complaints for pitch cable failures related to forceps and small Graptor instruments.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0923-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-12-19 |
| Published | 2025-01-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Intuitive Surgical |
| Distribution | US |
Product
8MM, Tenaculum Forceps REF 470207 Instrument used with the da Vinci X/Xi Surgical Systems in a wide variety of procedures to perform a variety of surgical tasks including manipulation and retraction of tissue.
Reason
Due to an increase in complaints for pitch cable failures related to forceps and small Graptor instruments
Identifiers
| code_info | Product Number: 470207 UDI-Di code: 00886874112366 Part Number and Version: 470207-04 Lot Numbers: S10131217 S10131218…Product Number: 470207 UDI-Di code: 00886874112366 Part Number and Version: 470207-04 Lot Numbers: S10131217 S10131218 Part Number and Version: 470207-07 Lot Numbers: S10140619 S10140622 S10140626 S10140718 S10140811 S10140912 S10141113 S10141121 S10150117 S10150202 Part Number and Version: 470207-08 Lot Numbers: N10160112 N10160128 N10160219 N10160316 N10160407 N10160420 N10160629 N10160705 N10160802 N10160824 N10160830 N10160914 N10160929 N10161011 N10161103 N10161109 N10161129 N10161212 N10170111 N10170201 N10170217 N10170308 N10170410 N10170509 N10170517 N10170612 N10170623 N10170705 N10170720 N10170809 N10170821 N10170829 N10170908 N10170927 N10171123 N10171204 N10180108 N10180119 N10180307 N10180308 N10180322 N10180404 N10180423 N10180516 N10180523 N10180528 N10180605 N10180613 S10141219 S10150207 S10150213 S10150310 S10150401 S10150416 S10150505 S10150518 S10150520 S10150618 S10150707 S10150715 S10150825 S10150903 S10150923 S10151002 S10160106 S10160120 S10160129 S10160225 S1 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0923-2025%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.