CLASS II Food recall · Reported 28 Nov 2012 · FDA Enforcement Report
Activia Light Nonfat Yogurt Peach Flavor recalled by The Dannon Company
The Dannon is recalling Activia Light Nonfat Yogurt Peach Flavor, Each unit of cups/6 pack to a case/case), distributed in Puerto Rico. The recall was initiated on 5 Oct 2012 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-0704-2013
- FDA event ID
- 63482
- Recalling firm
- The Dannon, Minster, OH
- Brand
- Activia
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 5 Oct 2012
- FDA classified
- 16 Nov 2012
- Reported
- 28 Nov 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Yogurt
Timeline
| 5 Oct 2012 | Recall initiated by company | |
| 16 Nov 2012 | Classified by FDA | +42 days |
| 28 Nov 2012 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Not labeled correctly
Product as listed by the FDA
Dannon Activia LIGHT Nonfat Yogurt Peach Flavor, Each unit 4-pack of 4-oz cups/6, 4-count pack to a case (24 cups/case) UPC 3663202633
Where it was distributed
21 US states and Puerto Rico
Questions about this recall
Why was it recalled?
Not labeled correctly
Which lots are affected?
Expiration Code NOV 07 2012 MZ, Expiration Code NOV 09 2012 MZ, Expiration Code NOV 10 2012 MZ
Where was it sold?
21 US states and Puerto Rico
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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