FDA Device recall Z-0873-2025
8MM,CADIERE FORCEPS,IS4000 REF 471049
- FDA Device
- Class II
- ongoing
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of 8MM,CADIERE FORCEPS,IS4000 REF 471049 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-0873-2025 |
| 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,CADIERE FORCEPS,IS4000 REF 471049
Reason
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Identifiers
| code_info | Model Number: 471049 Part Number: 471049-08 UDI-DI code: 00886874119778 Batch Numbers: K10221218 K10230112 K10230122 K1…Model Number: 471049 Part Number: 471049-08 UDI-DI code: 00886874119778 Batch Numbers: K10221218 K10230112 K10230122 K10230219 K10230226 K10230302 K10230323 K10230405 K10230413 K10230420 K10230427 K10230515 K10230518 K10230525 K10230608 K10230615 K10230622 K10230706 K10230713 K10230714 K10230720 K10230727 K10230803 K10230817 K10230921 K10230928 K10231005 K10231012 K10231027 K10231109 K10231130 K10231205 K10231207 K10231214 K10231218 K10240104 K10240110 K10240111 K10240116 K10240118 K10240208 K10240215 K10240222 K10240308 K10240321 K10240327 K10240404 K10240411 K10240418 K10240509 K10240516 K10240530 K10240606 K10240613 K10240614 K10240620 K10240621 K10240711 K10240718 K10240725 K10240903 K11230112 K11230226 K11230405 K11230515 K11230518 K11230525 K11230608 K11230615 K11230622 K11230706 K11230713 K11230714 K11230720 K11230727 K11230803 K11230817 K11230921 K11230928 K11231012 K11231027 K11231109 K11231130 K11231207 K11231214 K11240104 K11240118 K11240208 K11240215 K11240321 K11240327 K11 |
|---|
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-0873-2025%22
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