Potato Tater Puffs (Lamb Weston) – Plastic Contamination (2019)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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***".
Brand
Lamb Weston BSW LLC
Lot Codes / Batch Numbers
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.
Products Sold
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.
Lamb Weston BSW LLC is recalling Lamb s Supreme Potato Tater Puffs, item # H30, packaged in 5-pound unprinted KRAFT paper bags, 6 bag due to Formed Potato Tater Puffs (H30 s), sold as a foodservice item, are recalled due to contamination with plastic object.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Formed Potato Tater Puffs (H30 s), sold as a foodservice item, are recalled due to contamination with plastic object.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, CT, DE, FL, GA, IN, KY, MD, MA, MI, NH, NJ, NY, NC, OH, PA, RI, SC, VA, WI
Page updated: Jan 6, 2026