Class II — ASO, LLC
| Recalling firm | ASO LLC |
|---|---|
| Registered facility | View this company's 4 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Potential that gauze pads may not be fully sterilized |
| Product | Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in, 10 CT. White, bleached, non-woven, rayon/polyester sterile Gauze Pad 3 inch x 3 inch, 12-ply 10 count cardboard box |
| Quantity | 218 cases (72, 10-ct boxes per case) |
| Distribution | Distributed nationwide to AR, FL, IA, IN, KY, NY, OK, TX, UT, VA. |
| Initiated | 2018-10-16 |
| Classified | 2018-11-30 |
| Recall number | Z-0525-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — ASO, LLC (Z-0525-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/81555/
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