CLASS II Food recall · Reported 15 Oct 2025 · FDA Enforcement Report
Sadecki Bartnik Pylek Kwiatowy (Bee Pollen) glass recalled
Gospodarstwo Pasieczne Sadecki Bartnik is recalling Sadecki Bartnik Pylek Kwiatowy (Bee Pollen) glass, distributed in Illinois. The recall was initiated on 4 Sep 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
- H-0012-2026
- FDA event ID
- 97636
- Recalling firm
- Gospodarstwo Pasieczne Sadecki Bartnik, Grybow
- Brand
- Sadecki Bartnik
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 4 Sep 2025
- FDA classified
- 3 Oct 2025
- Reported
- 15 Oct 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Foreign Material
- Product category
- Other
Timeline
| 4 Sep 2025 | Recall initiated by company | |
| 3 Oct 2025 | Classified by FDA | +29 days |
| 15 Oct 2025 | 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
detectable pyrrolizidine alkaloids
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
Sadecki Bartnik Pylek Kwiatowy (Bee Pollen) 200g (7.05oz) glass jar UPC 5 900597 000788
Where it was distributed
IL
Questions about this recall
Why was it recalled?
detectable pyrrolizidine alkaloids
Which lots are affected?
13/12/2026 1/1
Where was it sold?
IL
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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