FDA Drug recall D-0250-2019
puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0
- FDA Drug
- Class I
- terminated
- Published 2018-11-21
On 2018-11-21 the FDA classified a Class I recall of puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0 by Kadesh International, citing non-Sterility: Product manufactured under non-sterile production conditions.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0250-2019 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2018-11-05 |
| Published | 2018-11-21 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Kadesh International |
| Distribution | US |
Product
puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.
Reason
Non-Sterility: Product manufactured under non-sterile production conditions.
Identifiers
| upc | 736972167990 |
|---|---|
| code_info | All lots, no expiration dates are on the bottles. |
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-0250-2019%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.