CLASS I Food recall · Reported 23 Aug 2017 · FDA Enforcement Report
Acidophilus-Plus, No. 102, Dietary Supplement recalled
NatureAll-STF Holding is recalling Acidophilus-Plus, No. 102, Dietary Supplement, distributed nationwide in the US. The recall was initiated on 26 Jul 2017 and the FDA has classified it as Class I.
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-3367-2017
- FDA event ID
- 77831
- Recalling firm
- NatureAll-STF Holding, Salt Lake City, UT
- Brand
- Acidophilus-Plus
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 26 Jul 2017
- FDA classified
- 14 Aug 2017
- Reported
- 23 Aug 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Allergens
- Product category
- Dietary Supplements
Timeline
| 26 Jul 2017 | Recall initiated by company | |
| 14 Aug 2017 | Classified by FDA | +19 days |
| 23 Aug 2017 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,
Where it was distributed
Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
Nationwide CaliforniaFloridaGeorgiaIdahoIllinoisIndianaTexasUtahVirginiaWashingtonWyoming
Questions about this recall
Is Acidophilus-Plus, No. 102, Dietary Supplement recalled?
Yes. NatureAll-STF Holding recalled Acidophilus-Plus, No. 102, Dietary Supplement on 26 Jul 2017. The recall is Class I and its status is Terminated. Recall number F-3367-2017.
Why was it recalled?
Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).
Which lots are affected?
Lot 43200916, Exp 9/2019
Where was it sold?
Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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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