FDA Drug recall D-0859-2021
Occular Allergy Blend 87% Alcohol
- FDA Drug
- Class II
- terminated
- Published 2021-10-06
On 2021-10-06 the FDA classified a Class II recall of Occular Allergy Blend 87% Alcohol by Washington Homeopathic Products, citing out-of-specification test results obtained for identification testing based on HPTLC analysis.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0859-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-08-20 |
| Published | 2021-10-06 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Washington Homeopathic Products |
| Distribution | US |
Product
Occular Allergy Blend 87% Alcohol; In Equal Parts of Apis Mellifica 7x Allium Cepa 7x Euphrasia Officinalis 7X Sabadilla 7X, WHP Homeopathic Medicine For Manufacturing Only, 500 ml. Manufcatured by Washington Homeopathic Products 260JR Hawvermale Way, Berkeley Springs WV 25411
Reason
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Identifiers
| code_info | Lot # 30148 |
|---|
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-0859-2021%22
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