INCISION & DRAINAGE TRAY or KIT — Class II medical device recall Z-1088-2018
Terminated recall by Centurion Medical Products Corporation, reported 2018-03-28. Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level req
| Recall number | Z-1088-2018 |
|---|---|
| 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 | 2017-10-23 |
| Classified | 2018-03-17 |
| Reported by FDA | 2018-03-28 |
| Terminated | 2018-06-21 |
| Reason classes | potency |
| Lot numbers | 2015081190, 2015091790, 2015092490, 2015100890, 2015101490, 2015101590, 2015102190, 2015102790, 2015103090, 2015110590, 2015111990, 2015112590, 2015121490, 2015121590, 2016010490, 2016010690, 2016010790, 2016011590, 2016012190, 2016020890, 2016021890, 2016022390, 2016022490, 2016022590, 2016030790, 2016031190, 2016031590, 2016031790, 2016033190, 2016040690, 2016042090, 2016042790, 2016051890, 2016052490, 2016052590, 2016060690, 2016060890, 2016061090, 2016061390, 2016062190 and 59 more |
Product
INCISION & DRAINAGE TRAY or KIT
Reason for recall
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
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-1088-2018. 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.