CLASS II Food recall · Reported 20 Nov 2013 · FDA Enforcement Report
Apotheca Energique Gastrozyme, dietary supplement recalled by Grato
Grato is recalling Apotheca Energique Gastrozyme, dietary supplement, distributed nationwide in the US. The recall was initiated on 1 Oct 2013 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0164-2014
- FDA event ID
- 66443
- Recalling firm
- Grato, Woodbine, IA
- Brand
- Apotheca Energique
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 1 Oct 2013
- FDA classified
- 12 Nov 2013
- Reported
- 20 Nov 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Other Reasons
- Product category
- Dietary Supplements
Timeline
| 1 Oct 2013 | Recall initiated by company | |
| 12 Nov 2013 | Classified by FDA | +42 days |
| 20 Nov 2013 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The products may contain chloramphenicol.
Product as listed by the FDA
Apotheca Energique Gastrozyme, dietary supplement, 100 vegetarian capsules.
Where it was distributed
Distribution was nationwide through retail and internet sales. The distribution list is pending.
Questions about this recall
Why was it recalled?
The products may contain chloramphenicol.
Which lots are affected?
Lot number C3354 The product mathmatical analysis of potential Chloramphenicol level is 1.07 ppb.
Where was it sold?
Distribution was nationwide through retail and internet sales. The distribution list is pending.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
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 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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