Valencian Almonds FS Skinless, MZ502, packaged in bulk package 5 KG. Net Wt. 352 oz./22 lb. (2 bags @ 11 lb.). UPC 5 901234 123457. ...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1058-2022.
Potential contamination with peanut while label does not declare peanut.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1058-2022.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Power Selles Imports Dba Culinary Collective or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1058-2022.
Power Selles Imports dba Culinary Collective
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Power Selles Imports Dba Culinary Collective Recall FAQ
Power Selles Imports Dba Culinary Collective is the subject of a dairy safety report: Valencian Almonds FS Skinless, MZ502, packaged in bulk package 5 KG. Net Wt. 352 oz./22 lb. (2 bags @ 11 lb.). UPC 5 901234 123457. .... The notice was published on May 5, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 78 units are potentially affected.