FDA Device recall Z-1733-2017
EYE KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer
- FDA Device
- Class II
- terminated
- Published 2017-04-12
On 2017-04-12 the FDA classified a Class II recall of EYE KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer by Centurion Medical Products, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1733-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-09 |
| Published | 2017-04-12 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Centurion Medical Products |
| Distribution | CA, IL, NC, NJ, NY, OH, PA, VA, WA |
Product
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.
Identifiers
| code_info | Centurion component code 2841, Affected product was placed into Centurion Convenience Kits between July 2013 and Januar…Centurion component code 2841, Affected product was placed into Centurion Convenience Kits between July 2013 and January 2017. Batch Numbers & Exp. dates: 2013120690 7/31/18 2013071890 10/31/17 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1733-2017%22
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