Arizona Nutritional Supplements Recall: Whey Protein Powder was mistakenly packaged with Soy Protein Powder. - F-0747-2021
United States
TerminatedClass I
- Company
- Arizona Nutritional Supplements
- Product
- 365 Everyday Value Whey Protein Powder Natural Vanilla Flavo…
- Recall date
- May 5, 2021
- Terminated
- February 9, 2022
- Source
- FDA
Reason for recall
Whey Protein Powder was mistakenly packaged with Soy Protein Powder.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 365 Everyday Value Whey Protein Powder Natural Vanilla Flavor, Net Wt. 13.9 oz. canisters, UPC 9948228764, Whole Foods Market 550 Bowie Street Austin, TX 78703. Store in a cool, dry place. | 9948228764 | 6,060 Canisters | Lot: 0073984; Best By: 03/04/2023 |
Distribution
- Nationwide.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0747-2021
- Event ID
- 87902
- Status
- Terminated
- Classification
- Class I
- Company
- Arizona Nutritional Supplements
- Product description
- 365 Everyday Value Whey Protein Powder Natural Vanilla Flavor, Net Wt. 13.9 oz. canisters, UPC 9948228764, Whole Foods Market 550 Bowie Street Austin, TX 78703. Store in a cool, dry place.
- Quantity
- 6,060 Canisters
- Reason
- Whey Protein Powder was mistakenly packaged with Soy Protein Powder.
- Recall initiation date
- May 5, 2021
- Report date
- June 16, 2021
- Classification date
- Not published in this source record
- Termination date
- February 9, 2022
- Distribution pattern
- Nationwide.
- UPC, lot, and code information
- UPC 9948228764; Lot: 0073984; Best By: 03/04/2023
- 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: Arizona Nutritional Supplements
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of February 9, 2022.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.