Class IITerminatedVoluntary: Firm initiated

Italianway Import, Inc.: food recall H-0540-2026

Italianway Import, Inc. of Hialeah, FL recalled VERGANI 1944 MILANO 'PANDORO CLASSICO' Gluten Free, 600g NET WT. 1 LBS. 5.2 OZ., packaged in paper cartons, 6 units… Reason: Potential contamination with foreign material (Teflon fragments) from flaking cooking molds. The FDA listed it as Class II in its Enforcement Report dated Mar 11, 2026; distribution: Florida, Michigan, New Jersey.

Record status as published: Terminated (terminated May 28, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
VERGANI 1944 MILANO 'PANDORO CLASSICO' Gluten Free, 600g NET WT. 1 LBS. 5.2 OZ., packaged in paper cartons, 6 units per case. Lot 217666, UPC 8002114019833
Product quantity
10 cases (6 units/ case) Total: 60 units (600g each)
Reason for recall
Potential contamination with foreign material (Teflon fragments) from flaking cooking molds.
Codes, lots and dates on the package
Lot code: L217666 Expiration: 04/08/2026
Distribution pattern
Distributed in: FL, MI, NJ
Recalling firm
Italianway Import, Inc., Hialeah, FL
Classification
Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
E-Mail

Dates

EventDate
Recall initiated by the firmFeb 10, 2026
Classified by the FDAMar 4, 2026
Published in the Enforcement ReportMar 11, 2026
TerminatedMay 28, 2026

All food recall records

OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.

Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0540-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.