Avanti Frozen Foods Private Limited Recall: One lot of uncooked shrimp was inadvertently packaged as cooked shrimp. - F-0437-2021
United States
TerminatedClass III
- Company
- Avanti Frozen Foods Private Limited
- Product
- 365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready…
- Recall date
- March 20, 2021
- Terminated
- April 28, 2021
- Source
- FDA
Reason for recall
One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- to - Serve Tail-On/Peeled & Deveined/41-55 Shrimp/lb NET WT 32 OZ (2 LB) 907g packaged in clear plastic bag | Not published in this source record | 8,290 packages | PRODUCTION DATE CODE: 91AS/22VN/175A |
Distribution
- Potentially Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0437-2021
- Event ID
- 87589
- Status
- Terminated
- Classification
- Class III
- Company
- Avanti Frozen Foods Private Limited
- Product description
- 365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- to - Serve Tail-On/Peeled & Deveined/41-55 Shrimp/lb NET WT 32 OZ (2 LB) 907g packaged in clear plastic bag
- Quantity
- 8,290 packages
- Reason
- One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.
- Recall initiation date
- March 20, 2021
- Report date
- April 28, 2021
- Classification date
- Not published in this source record
- Termination date
- April 28, 2021
- Distribution pattern
- Potentially Nationwide
- UPC, lot, and code information
- PRODUCTION DATE CODE: 91AS/22VN/175A
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Avanti Frozen Foods Private Limited
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.
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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?
FDA classifies this recall as Class III. 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 April 28, 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.
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