Product Wiki · Recalls · U.S. FDA — Device Enforcement

Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the Intuitive Surgical Da Vinci Si Robotic system / Distributed by Intuitive Surgical Product Usage: Microtek Medical Equipment Drapes are intended to cover/wrap various surgical and/or n — recall Z-0232-2019

U.S. FDA — Device Enforcement · United States · 2018-09-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0232-2019
Date of alert
2018-09-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ecolab Inc
Product category
device
Product type
Devices
Reported risk: The pouches of certain lots of product may have wrinkles along the pouch seal that could result in a channel within the seal. Should there be a channel in the pouch seal it may result in a breach in the sterility of the product.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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