FDA Drug recall D-0300-2018
Medline Debridement Tray, Sterile, Single Use Only
- FDA Drug
- Class II
- terminated
- Published 2018-02-07
On 2018-02-07 the FDA classified a Class II recall of Medline Debridement Tray, Sterile, Single Use Only by Medline Industries, citing subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0300-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-09-21 |
| Published | 2018-02-07 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Medline Debridement Tray, Sterile, Single Use Only. Assembled in USA by Medline Industries, Inc., Mundelein, IL 6060
Reason
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Identifiers
| code_info | Pack Number: DYNDW1032 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0300-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.