FDA Device recall Z-0847-2025
8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179
- FDA Device
- Class II
- ongoing
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of 8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179 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-0847-2025 |
| 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, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179
Reason
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Identifiers
| code_info | Model Number: 470179 Part Number: 470179-19 UDI-DI code: 00886874112298 Batch Number: K10221127 K10221218 K10221228 K10…Model Number: 470179 Part Number: 470179-19 UDI-DI code: 00886874112298 Batch Number: K10221127 K10221218 K10221228 K10230103 K10230108 K10230112 K10230122 K10230129 K10230205 K10230212 K10230219 K10230226 K10230302 K10230310 K10230315 K10230316 K10230323 K10230330 K10230403 K10230405 K10230412 K10230413 K10230420 K10230504 K10230509 K10230511 K10230516 K10230518 K10230525 K10230531 K10230601 K10230602 K10230608 K10230615 K10230620 K10230622 K10230629 K10230630 K10230706 K10230713 K10230720 K10230727 K10230803 K10230810 K10230817 K10230824 K10230831 K10230907 K10230914 K10230921 K10230928 K10231005 K10231006 K10231012 K10231019 K10231026 K10231102 K10231109 K10231123 K10231130 K10231207 K10231213 K10231214 K10231218 K10240104 K10240111 K10240118 K10240125 K10240201 K10240208 K10240215 K10240222 K10240229 K10240301 K10240307 K10240314 K10240315 K10240321 K10240327 K10240410 K10240411 K10240418 K10240425 K10240426 K10240502 K10240515 K10240516 K10240523 K10240530 K10240605 K10240606 K102 |
|---|
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-0847-2025%22
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