POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye… — Class II medical device recall Z-1734-2017
Terminated recall by Centurion Medical Products Corporation, reported 2017-04-12, distributed in CA, IL, NC, NJ, NY, OH, PA, VA…. Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to sup
| Recall number | Z-1734-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Centurion Medical Products Corporation, Williamston, MI, United States |
| Recall initiated | 2017-03-09 |
| Classified | 2017-04-05 |
| Reported by FDA | 2017-04-12 |
| Terminated | 2017-08-07 |
| Distributed | CA, IL, NC, NJ, NY, OH, PA, VA, WA |
| Quantity | 45 kits |
| Reason classes | sterility |
| Lot numbers | 2014082550, 2015052650, 2016020950 |
Product
POST-OPERATIVE OPHTHALMIC DRESSING TRAY 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1734-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.