Medline Suture Removal Tray — Class II drug recall D-0317-2018
Terminated recall by Medline Industries Inc, reported 2018-02-07, distributed nationwide. Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
| Recall number | D-0317-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2017-09-21 |
| Classified | 2018-02-04 |
| Reported by FDA | 2018-02-07 |
| Terminated | 2023-08-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CL, CN, HN, IL, IN, MX, MY, TR |
| Quantity | 9,000 cases |
| Reason classes | labeling, potency |
| Lot numbers | 16KB5621, 17CB8694, 17MB4778 |
Product
Medline Suture Removal Tray, Sterile, Single Use Only. Packaged in USA for Medline Industries, Inc., Mundelein, IL 60060
Reason for recall
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
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/D-0317-2018. 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.