FDA Device recall Z-0875-2025
8MM,MICRO BIPOLAR FORCEPS,IS4000 REF 471171
- FDA Device
- Class II
- ongoing
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of 8MM,MICRO BIPOLAR FORCEPS,IS4000 REF 471171 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-0875-2025 |
| 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,MICRO BIPOLAR FORCEPS,IS4000 REF 471171
Reason
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Identifiers
| code_info | Model Number: 471171 Part Number: 471171-15 UDI-DI code: 00886874121474 Batch Numbers: K10230405 K10230413 K10230601 K1…Model Number: 471171 Part Number: 471171-15 UDI-DI code: 00886874121474 Batch Numbers: K10230405 K10230413 K10230601 K10230615 K10230713 K10230817 K10230907 K10230913 K10231103 K10231123 K10231130 K10231207 K10231214 K10231221 K10240104 K10240118 K10240208 K10240222 K10240327 K10240411 K10240502 K10240516 K10240702 K10240711 K16240508 K16240530 |
|---|
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-0875-2025%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.