CLASS III Drug recall · Reported 25 Nov 2020 · FDA Enforcement Report
Homeopathic Energy Catalyst recalled by Grato Holdings
Grato Holdings is recalling Homeopathic Energy Catalyst, distributed in Utah. The recall was initiated on 17 Sep 2020 and the FDA has classified it as Class III.
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-0099-2021
- FDA event ID
- 86690
- Recalling firm
- Grato Holdings, Woodbine, IA
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 17 Sep 2020
- FDA classified
- 19 Nov 2020
- Reported
- 25 Nov 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Labeling Errors
Timeline
| 17 Sep 2020 | Recall initiated by company | |
| 19 Nov 2020 | Classified by FDA | +63 days |
| 25 Nov 2020 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Product Contains Undeclared API; Incorrect formulation
Product as listed by the FDA
Homeopathic Energy Catalyst, 1 fl oz (30 mL) Distributed by: Deseret Biologicals, Inc. 469 W. Parkland Drive Sandy, UT 84070. NDC 43742-0756-1.
Where it was distributed
UT
Questions about this recall
Why was it recalled?
Labeling: Product Contains Undeclared API; Incorrect formulation
Which lots are affected?
Lot #s: Z60852, Z60012
Where was it sold?
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 III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 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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