RecallRadar

FDA Device recall Z-0866-2025

8MM,SMALL GRASPING RETRACTOR,IS4000¿ REF 470318

On 2025-01-22 the FDA classified a Class II recall of 8MM,SMALL GRASPING RETRACTOR,IS4000¿ REF 470318 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

AgencyFDA Device
Recall numberZ-0866-2025
ClassificationClass II
Statusongoing
Initiated2024-12-19
Published2025-01-22
Last updated2026-09-13 11:57 UTC
CompanyIntuitive Surgical
DistributionAK, 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,SMALL GRASPING RETRACTOR,IS4000¿ REF 470318

Reason

Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.

Identifiers

code_info
Model Number: 470318 Part Number: 470318-10 UDI-DI code: 00886874112441 Batch Numbers: K10230212 K10230219 K10230226 K1…Model Number: 470318 Part Number: 470318-10 UDI-DI code: 00886874112441 Batch Numbers: K10230212 K10230219 K10230226 K10230420 K10230504 K10230511 K10230518 K10230525 K10230601 K10230608 K10230615 K10230706 K10230713 K10230803 K10230817 K10230831 K10230914 K10230921 K10230928 K10231012 K10231019 K10231027 K10231130 K10231207 K10240104 K10240116 K10240125 K10240222 K10240327 K10240404 K10240516 K10240523 K10240606 K10240711 K10240725 K10240822 K10240829 K11230608

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-0866-2025%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.