FDA Device recall Z-0882-2025
8MM,LONG BIPOLAR GRASPER,IS4000 REF 471400
- FDA Device
- Class II
- ongoing
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of 8MM,LONG BIPOLAR GRASPER,IS4000 REF 471400 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-0882-2025 |
| 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,LONG BIPOLAR GRASPER,IS4000 REF 471400
Reason
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Identifiers
| code_info | Model Number: 471400 Part Number: 471400-10 UDI-DI code: 00886874121528 Batch Numbers: K10221106 K10221212 K10230129 K1…Model Number: 471400 Part Number: 471400-10 UDI-DI code: 00886874121528 Batch Numbers: K10221106 K10221212 K10230129 K10230205 K10230212 K10230219 K10230226 K10230413 K10230504 K10230515 K10230518 K10230525 K10230601 K10230608 K10230615 K10230630 K10230713 K10230720 K10230817 K10230824 K10230831 K10230913 K10230917 K10230928 K10231005 K10231012 K10231019 K10231027 K10231102 K10231130 K10231218 K10240104 K10240116 K10240208 K10240322 K10240327 K10240404 K10240411 K10240516 K10240523 K10240606 K10240613 K10240618 K11221106 K11230129 K11230515 K11230824 K11231012 K11240104 K11240404 K11240702 |
|---|
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-0882-2025%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.