FDA Device recall Z-0852-2025
8MM,DEBAKEY FORCEPS,IS4000 ¿ REF 470036
- FDA Device
- Class II
- ongoing
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of 8MM,DEBAKEY FORCEPS,IS4000 ¿ REF 470036 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-0852-2025 |
| 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,DEBAKEY FORCEPS,IS4000 ¿ REF 470036
Reason
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Identifiers
| code_info | Model Number: 470036 Part Number: 470036-04 UDI-DI code: 00886874112236 Batch Numbers: K10221128 K10221218 K10230219 K1…Model Number: 470036 Part Number: 470036-04 UDI-DI code: 00886874112236 Batch Numbers: K10221128 K10221218 K10230219 K10230226 K10230323 K10230518 K10230525 K10230601 K10230608 K10230615 K10230713 K10230824 K10230907 K10231005 K10231019 K10231214 K10240208 K10240222 K10240411 K10240418 K10240711 K10240722 K10240801 Part Number: 470036-06 UDI-DI code: 00886874112229 Batch Number: K10230803 |
|---|
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-0852-2025%22
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