FDA Drug recall D-900-2013
Nata Komplete, containing one 30-count bottle of multi-vitamin tablets (imprinted 909), Manufactured for W.H. Nutritionals, Wilmington, DE…
- FDA Drug
- Class III
- terminated
- Published 2013-08-28
On 2013-08-28 the FDA classified a Class III recall of Nata Komplete, containing one 30-count bottle of multi-vitamin tablets (imprinted 909), Manufactured for W.H. Nutritionals, Wilmington, DE… by Stayma Consulting Service, citing subpotent; Beta carotene (Vitamin A).
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-900-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-06-28 |
| Published | 2013-08-28 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Stayma Consulting Service |
| Distribution | US |
Product
Nata Komplete, containing one 30-count bottle of multi-vitamin tablets (imprinted 909), Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-909-30) and physician samples of nine bottles of 5-multi-vitamin tablets (NDC 76331-909-05 )
Reason
Subpotent; Beta carotene (Vitamin A)
Identifiers
| code_info | NDC 76331-909-30; Lot 40186, exp 5/14 NDC 76331-909-05; Lot 40186, exp. 5/14 (physician samples) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-900-2013%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.