FDA Food recall H-0521-2026
Aonic Complete His
- FDA Food
- Class II
- completed
- Published 2026-02-18
On 2026-02-18 the FDA classified a Class II recall of Aonic Complete His by Tks Pack Manufacturing, citing possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | H-0521-2026 |
| Classification | Class II |
| Status | completed |
| Initiated | 2026-01-15 |
| Published | 2026-02-18 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Tks Pack Manufacturing |
| Distribution | UT |
Product
Aonic Complete His. Dosage: Single serving liquid dietary supplement drink shot, 34 ml (1.1 Fl oz) in plastic bottle, induction sealed closed with plastic lid. Each bottle is a serving intended to be taken orally as a dietary supplement. Sipping unit: two 15 count decorated boxes in a corrugated Aonic Master Shipper. Firm Name and Address on Label: Aonic Inc. 2261 MarketStreet #5416 San Francisco, CA 94114 USA.
Reason
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Identifiers
| code_info | Lot 5349A BB 12/27; Lot 5363A BB 12/27 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0521-2026%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.