Eyesaline — Class II drug recall D-0461-2024
Terminated recall by HONEYWELL INC, reported 2024-05-01, distributed nationwide. CGMP Deviations
| Recall number | D-0461-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | HONEYWELL INC, Charlotte, NC, United States |
| Recall initiated | 2024-03-29 |
| Classified | 2024-04-23 |
| Reported by FDA | 2024-05-01 |
| Terminated | 2024-09-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Reason classes | cgmp |
| NDC | 00498-0631, 00498-0631-37 |
| Model numbers | 32-002050-0000 |
| Expiration dates | 2025-06-21 |
Product
Eyesaline, Saline Eyewash Solution, Cartridge for Fendall 2000, Net contents: 7.9 gal per cartridge, Sperian Eye & Face Protection, Inc., 825 East Highway 151, Platteville, WI 53818. NDC: 0498-0631-37
Reason for recall
CGMP Deviations
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-0461-2024. 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.