STEWARTS SHOPS CORP Recall: The specific code of SPORTADE FRUIT PUNCH may contain undeclared milk.
United States
TerminatedClass I
- Company
- STEWARTS SHOPS CORP
- Product
- Stewart's SPORTADE FRUIT PUNCH Isotonic Beverage 20 Fl Oz (5…
- Recall date
- October 26, 2016
- Terminated
- December 12, 2016
- Source
- FDA
Reason for recall
The specific code of SPORTADE FRUIT PUNCH may contain undeclared milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Stewart's SPORTADE FRUIT PUNCH Isotonic Beverage 20 Fl Oz (591 mL), UPC 0 82086 31006 8. The product is packaged in a plastic bottle, and has a black label with a red plastic cap. | Not published in this source record | 1622 bottles | Expiration date code DEC 02 (found on the neck of the bottle) |
Distribution
- Upstate New York and Southern Vermont
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0501-2017
- Event ID
- 75547
- Status
- Terminated
- Classification
- Class I
- Company
- STEWARTS SHOPS CORP
- Product description
- Stewart's SPORTADE FRUIT PUNCH Isotonic Beverage 20 Fl Oz (591 mL), UPC 0 82086 31006 8. The product is packaged in a plastic bottle, and has a black label with a red plastic cap.
- Quantity
- 1622 bottles
- Reason
- The specific code of SPORTADE FRUIT PUNCH may contain undeclared milk.
- Recall initiation date
- October 26, 2016
- Report date
- November 30, 2016
- Classification date
- Not published in this source record
- Termination date
- December 12, 2016
- Distribution pattern
- Upstate New York and Southern Vermont
- UPC, lot, and code information
- Expiration date code DEC 02 (found on the neck of the bottle)
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: STEWARTS SHOPS CORP
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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
