Lamb s Supreme Potato Tater Puffs recall
Recalled by Lamb Weston BSW LLC · Warden, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Formed Potato Tater Puffs (H30 s), sold as a foodservice item, are recalled due to contamination with plastic object.
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
Lamb s Supreme Potato Tater Puffs, item # H30, packaged in 5-pound unprinted KRAFT paper bags, 6 bags to a case, sold as a foodservice item. UPC 1 00 44979 00830 5. The case label is read in parts: "***LAMB'S SUPREME TATER PUFFS***FROZEN POTATOES***6/5 LB BAGS***Produced by Lamb Weston, 8701 W. Gage Blvd. Kennewick, WA***".
Quantity: 22,789 cases
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 code: 616001092121HH.MM; 616001102121HH.MM; 616001112121HH.MM; 616001122121HH.MM; 616001132121HH.MM; 616001142121HH.MM; Expiration Dates: 2020.07.09; 2020.07.10; 2020.07.11; 2020.07.12; 2020.07.13; 2020.07.14.
Where it was sold
Alabama Connecticut Delaware Florida Georgia Kentucky Massachusetts Maryland Michigan North Carolina New Hampshire New Jersey New York Ohio Pennsylvania Rhode Island South Carolina Virginia Wisconsin
FDA's distribution note: distributed in AL, CT, DE, FL, GA, KY, MA, MD, MI, NC, NH, NJ, NY, OH, PA, RI, SC, VA, and WI.
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
- Lamb Weston BSW LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 10, 2019
- In FDA report of
- May 8, 2019
- Terminated
- Jul 2, 2019
- FDA recall number
- F-1321-2019 · event 82622
- Official record
- FDA enforcement report search