CLASS II Food recall · Reported 1 Sep 2021 · FDA Enforcement Report
Assist and Amend Advanced Digestive Enzyme Formula recalled
New Dawn Nutrition is recalling Assist and Amend Advanced Digestive Enzyme Formula, Dietary Supplement per. The recall was initiated on 16 Jul 2021 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-0886-2021
- FDA event ID
- 88332
- Recalling firm
- New Dawn Nutrition, Omaha, NE
- Brand
- Assist
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 16 Jul 2021
- FDA classified
- 26 Aug 2021
- Reported
- 1 Sep 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Milk
- Product category
- Probiotics
Timeline
| 16 Jul 2021 | Recall initiated by company | |
| 26 Aug 2021 | Classified by FDA | +41 days |
| 1 Sep 2021 | 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
Product contained undeclared milk, wheat, and soy.
Product as listed by the FDA
Assist and Amend Advanced Digestive Enzyme Formula, Dietary Supplement, 60 capsules per bottle, Manufactured for and distributed by New Dawn Nutrition Omaha, NE
Where it was distributed
Distributed to two retail consumers in the Omaha area.
Questions about this recall
Why was it recalled?
Product contained undeclared milk, wheat, and soy.
Which lots are affected?
Lot #361551 Best By 2022
Where was it sold?
Distributed to two retail consumers in the Omaha area.
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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