Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported May 7, 2014
Pastene ITAL NIDI #81 ,16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7090 UPC: 066086070900
Semolina pasta fails to declare the allergen"wheat"
The recall
The Pastene Companies Ltd. issued this moderate-severity FDA Food recall — Semolina pasta fails to declare the allergen"wheat".
- Moderate
- severity level
- Class II
- classification
- May 7, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1905-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1905-2014) was formally reported on May 7, 2014, with the manufacturer initiating the action on April 10, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. The Pastene Companies Ltd. is listed as the recalling firm, operating out of Canton, MA. Federal records list the affected scope as 6,000 cases, total for all varieties.
The documented reason for this recall is: Semolina pasta fails to declare the allergen"wheat" Distribution data in the federal record shows the product reached: Nationwide Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category — 22,938 food recalls on record
Where this recall sits in the database
Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified moderate severity.
Affected scope
6,000 cases, total for all varieties
Related Recalls
6
6 from same agency
Product description
Pastene ITAL NIDI #81 ,16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7090 UPC: 066086070900
Reason for recall
Semolina pasta fails to declare the allergen"wheat"
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1905-2014 |
| Date reported | May 7, 2014 |
| Date initiated | April 10, 2014 |
| Recalling firm | The Pastene Companies Ltd. |
| Firm location | Canton, MA |
| Affected scope | 6,000 cases, total for all varieties |
| Distribution | Nationwide Nationwide |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
Frequently Asked Questions
What product was recalled? ▼
Pastene ITAL NIDI #81 ,16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7090 UPC: 066086070900. Recalled by The Pastene Companies Ltd.. Units affected: 6,000 cases, total for all varieties.
Why was this product recalled? ▼
Semolina pasta fails to declare the allergen"wheat"
Which agency issued this recall? ▼
This recall was issued by the FDA Food on May 7, 2014. Severity: Moderate. Recall number: F-1905-2014.
Where was the recalled product distributed? ▼
Distribution: Nationwide Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1905-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported May 7, 2014.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).