CLASS II Food recall · Reported 26 Mar 2025 · FDA Enforcement Report
emd Oysterettes (oyster crackers in polypropylene film) recalled
Dairy State Foods is recalling emd Oysterettes (oyster crackers in polypropylene film), distributed in Michigan. The recall was initiated on 12 Mar 2025 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-0642-2025
- FDA event ID
- 96525
- Recalling firm
- Dairy State Foods, Milwaukee, WI
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Mar 2025
- FDA classified
- 19 Mar 2025
- Reported
- 26 Mar 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Foreign Material
- Product category
- Crackers
Timeline
| 12 Mar 2025 | Recall initiated by company | |
| 19 Mar 2025 | Classified by FDA | +7 days |
| 26 Mar 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Foreign object (metal)
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
emd Oysterettes (oyster crackers in polypropylene film). 0.75 oz. Packed for and Distributed by emd, Detroit, MI 48212.
Where it was distributed
MI
Questions about this recall
Why was it recalled?
Foreign object (metal)
Which lots are affected?
Date Codes: 34824 and 35324
Where was it sold?
MI
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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