Z-1736-2017 Class II Terminated
FDA device recall Z-1736-2017 was initiated by Centurion Medical Products Corporation on March 9, 2017 and is designated Class II. Reason for recall: Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging. The recall status is terminated (terminated August 7, 2017). Affected quantity: 540 kits.
Recall Details
- Product Type
- Devices
- Report Date
- April 12, 2017
- Initiation Date
- March 9, 2017
- Termination Date
- August 7, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 540 kits
Product Description
CUSTOM CADAVER KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
Reason for Recall
Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.
Distribution Pattern
US Distribution: NY, NC, PA, CA, OH, WA, VA, NJ, IL
Code Information
Centurion component code 2841, Affected product was placed into Centurion Convenience Kits between July 2013 and January 2017. Batch Numbers & Exp. dates: 2016102103 1/31/20 2017012303 1/31/20 2016050203 1/31/20 2016040703 1/31/20 2016031803 1/31/20 2015112303 1/31/20 2015122103 1/31/20 2015050703 2/28/20 2015092803 1/31/20 2015081703 1/31/20 2015052003 1/31/20