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Recall

Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case

Cardinal Health 200, LLC · 28 July 2017

Status
Recall terminated
Why, in the FDA's words
“Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.”
Recall began
28 July 2017
Company
Cardinal Health 200, LLC
Device type
Product code (KKK)

What it means

A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.

The record

The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.
FDA database