FDA Device recall Z-0862-2025
8MM,ATRIAL RETRACTOR SHORT RIGHT,IS4000¿ REF 470246
- FDA Device
- Class II
- ongoing
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of 8MM,ATRIAL RETRACTOR SHORT RIGHT,IS4000¿ REF 470246 by Intuitive Surgical, citing due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0862-2025 |
| 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 | AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
Product
8MM,ATRIAL RETRACTOR SHORT RIGHT,IS4000¿ REF 470246
Reason
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Identifiers
| code_info | Model Number: 470246 Part Number: 470246-09 UDI-DI code: 00886874112397 Batch Numbers: K10230219 K10230226 K10230525 K1…Model Number: 470246 Part Number: 470246-09 UDI-DI code: 00886874112397 Batch Numbers: K10230219 K10230226 K10230525 K10230601 K10230608 K10230615 K10231218 K10240104 K10240111 K10240411 K10240613 K10240620 K10240711 K10240725 |
|---|
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-0862-2025%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.