Jason Pharmaceuticals, Inc. t/a Medifast Recall: The product contains undeclared milk. - F-0938-2020
United States
TerminatedClass I
- Company
- Jason Pharmaceuticals, Inc. t/a Medifast
- Product
- Optavia, Old Fashioned Maple & Brown Sugar Oatmeal . 1.13 o…
- Recall date
- May 1, 2020
- Terminated
- October 19, 2021
- Source
- FDA
Reason for recall
The product contains undeclared milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Optavia, Old Fashioned Maple & Brown Sugar Oatmeal . 1.13 oz./ 32 g pouch, Multi-layer Kraft paper/aluminum pouches, Seven pouches per carton | Not published in this source record | 24,923 cartons | RP1048870, RP1048871, RP1048886 with Best Buy dates of 01082021 and 01092021 |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0938-2020
- Event ID
- 85604
- Status
- Terminated
- Classification
- Class I
- Company
- Jason Pharmaceuticals, Inc. t/a Medifast
- Product description
- Optavia, Old Fashioned Maple & Brown Sugar Oatmeal . 1.13 oz./ 32 g pouch, Multi-layer Kraft paper/aluminum pouches, Seven pouches per carton
- Quantity
- 24,923 cartons
- Reason
- The product contains undeclared milk.
- Recall initiation date
- May 1, 2020
- Report date
- May 13, 2020
- Classification date
- Not published in this source record
- Termination date
- October 19, 2021
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- RP1048870, RP1048871, RP1048886 with Best Buy dates of 01082021 and 01092021
- 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: Jason Pharmaceuticals, Inc. t/a Medifast
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
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How to interpret this historical record
This record is preserved as published by FDA, as of October 19, 2021.
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.