FDA Recall
Terminated
EYE 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.
Recall: Z-1733-2017
·
Initiated March 9, 2017
Recall
- Recall Number
- Z-1733-2017
- Event Number
- 76730
- Firm
- Centurion Medical Products Corporation
- FEI Number
- 3008403546
- Product Code
- OXQ
- Status
- Terminated
- Root Cause
- Nonconforming Material/Component
- Initiated
- March 9, 2017
- Posted
- March 27, 2017
- Terminated
- August 7, 2017
- Address
- 100 Centurion Way, Williamston, MI, 48895-9086
Description
EYE 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
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.
Action
On March 9, 2017 Centurion Medical Products recalled specific lots of medical convenience kits due to a supplier initiated recall of Covidien Curity Eye Pads. All affected customers were notified, advised to discontinue use of associated kits, and requested to confirm the status of remaining stock to Centurion.
Distribution
US Distribution: NY, NC, PA, CA, OH, WA, VA, NJ, IL
Quantity
120 kits