Z-3046-2017 Class II Terminated
FDA device recall Z-3046-2017 was initiated by Cardinal Health 200, LLC on July 28, 2017 and is designated Class II. Reason for recall: Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings. The recall status is terminated (terminated December 26, 2017). Affected quantity: 200 units.
Recall Details
- Product Type
- Devices
- Report Date
- August 30, 2017
- Initiation Date
- July 28, 2017
- Termination Date
- December 26, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 200 units
Product Description
Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case
Reason for Recall
Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.
Distribution Pattern
US Distribution to the states of : NC, UT, OR, NY,TX, GA, NJ and FL.
Code Information
Lot number 17DAH349