Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
PF Chang's Home Menu Brand Shrimp Lo Mein recall
Recalled by ConAgra Frozen Foods, Inc · Russellville, AR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Metal fragments were discovered in an raw ingredient used in the manufacture of frozen meal products
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
PF Chang's Home Menu Brand Shrimp Lo Mein, UPC 3100067005, 22 oz bag, 4 bags per case, ConAgra Foods, Omaha, NE 68102
Quantity: 2,969/4/22 OZ/bags/cases
Food: Seafood & fish
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot number 5006616700, best by 6/10/2017
Where it was sold
Alabama Arizona Florida Georgia Louisiana Massachusetts Maryland Maine Mississippi North Carolina New Mexico New York Oregon Pennsylvania South Carolina Texas Virginia Washington
FDA's distribution note: Product was distributed to distributors in the following US state: AL, AZ, FL, GA, LA, MA, MD, ME, MS, NC, NM, NY, OR, PA, SC, TX, VA, and WA. No foreign or military/government distribution.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- ConAgra Frozen Foods, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 16, 2016
- In FDA report of
- Sep 14, 2016
- Terminated
- Feb 28, 2018
- FDA recall number
- F-2087-2016 · event 74717
- Official record
- FDA enforcement report search
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