FDA Device recall Z-0880-2025
8MM,MEGA SUTURECUT ND,IS4000 REF 471309
- FDA Device
- Class II
- ongoing
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of 8MM,MEGA SUTURECUT ND,IS4000 REF 471309 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-0880-2025 |
| 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,MEGA SUTURECUT ND,IS4000 REF 471309
Reason
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Identifiers
| code_info | Model Number: 471309 Part Number: 471309-15 UDI-DI code: 00886874119815 Batch Numbers: K10221113 K10221115 K10221212 K1…Model Number: 471309 Part Number: 471309-15 UDI-DI code: 00886874119815 Batch Numbers: K10221113 K10221115 K10221212 K10221218 K10230103 K10230112 K10230122 K10230124 K10230129 K10230205 K10230212 K10230219 K10230720 K10230824 K10240621 K10240718 K11221113 K11221115 K11221212 K11230103 K11230112 K11230122 K11230202 K11230212 K11230217 K12221113 K12221212 K12230112 K12230122 K12230205 K12230217 K13221113 K13230217 K14230217 K15230217 K16240508 K16240531 U10230217 U10230223 Model Number: 471309 Part Number: 471309-16 UDI-DI code: 00886874119815 Batch Numbers: K10230302 K10230310 K10230316 K10230323 K10230330 K10230413 K10230420 K10230427 K10230504 K10230509 K10230511 K10230518 K10230525 K10230601 K10230608 K10230615 K10230622 K10230630 K10230706 K10230713 K10230727 K10230803 K10230810 K10230817 K10230831 K10230913 K10230914 K10230921 K10231005 K10231012 K10231019 K10231027 K10231102 K10231109 K10231123 K10231130 K10231207 K10231218 K10240104 K10240111 K10240118 K10240125 K10240215 K1024 |
|---|
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-0880-2025%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.