ReliOn — Class II drug recall D-0602-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-09-03, distributed nationwide. Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
| Recall number | D-0602-2025 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2025-07-07 |
| Classified | 2025-08-26 |
| Reported by FDA | 2025-09-03 |
| Distributed | Nationwide (US) |
| Quantity | 3,456,000 pads |
| Reason classes | labeling, potency |
| NDC | 49035-0814, 49035-0814-30, 49035-0814-60 |
Product
ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs, Distributed by, Walmart, Inc., Bentonville, AR 72716 Walmart: 200 eaches per box, 24 boxes per case (4,800 eaches per case), NDC 49035-814-60.
Reason for recall
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
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-0602-2025. 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.