Empresas La Famosa, Inc. Recall: Discovered swollen cans
United States
TerminatedClass III
- Company
- Empresas La Famosa, Inc.
- Product
- Mr. Special Jugo de Pina De Concentrado, 46 oz cans, package…
- Recall date
- August 23, 2021
- Terminated
- March 9, 2022
- Source
- FDA
Reason for recall
Discovered swollen cans
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Mr. Special Jugo de Pina De Concentrado, 46 oz cans, packaged cardboard boxes 12 cans per case of 46 oz each | Not published in this source record | 409 cases 12/46 oz cans | P1105A2PDT03, Exp. Apr/ 15/ 2022 |
Distribution
- Domestic distribution only: Puerto Rico
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0216-2022
- Event ID
- 88881
- Status
- Terminated
- Classification
- Class III
- Company
- Empresas La Famosa, Inc.
- Product description
- Mr. Special Jugo de Pina De Concentrado, 46 oz cans, packaged cardboard boxes 12 cans per case of 46 oz each
- Quantity
- 409 cases 12/46 oz cans
- Reason
- Discovered swollen cans
- Recall initiation date
- August 23, 2021
- Report date
- December 1, 2021
- Classification date
- Not published in this source record
- Termination date
- March 9, 2022
- Distribution pattern
- Domestic distribution only: Puerto Rico
- UPC, lot, and code information
- P1105A2PDT03, Exp. Apr/ 15/ 2022
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Empresas La Famosa, Inc.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
