CLASS II Drug recall · Reported 9 Sep 2020 · FDA Enforcement Report
HGH Vitality Homeopathic recalled by Grato Holdings
Grato Holdings is recalling HGH Vitality Homeopathic, distributed in Utah. The recall was initiated on 16 Jul 2020 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1558-2020
- FDA event ID
- 86233
- Recalling firm
- Grato Holdings, Woodbine, IA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 16 Jul 2020
- FDA classified
- 29 Aug 2020
- Reported
- 9 Sep 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
Timeline
| 16 Jul 2020 | Recall initiated by company | |
| 29 Aug 2020 | Classified by FDA | +44 days |
| 9 Sep 2020 | Published in enforcement report | +11 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Error on Declared Strength
Product as listed by the FDA
HGH Vitality Homeopathic, 90 tablets, NDC 43742-1299-1, Dist. by Deseret Biologicals, Inc. 469 W. Parkland Drive, Sandy, UT 84070, NDC: 43742-1299-1
Where it was distributed
One direct account in UT
Questions about this recall
Is HGH Vitality Homeopathic recalled?
Yes. Grato Holdings recalled HGH Vitality Homeopathic on 16 Jul 2020. The recall is Class II and its status is Terminated. Recall number D-1558-2020.
Why was it recalled?
Labeling: Error on Declared Strength
Which lots are affected?
Lot P2613
Where was it sold?
One direct account in UT
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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