FDA recall record

Apple King Nature's Delight brand, packaged in tray pack box size 64, net recall — FDA F-0017-2018

Fuji apples are recalled because Thiabendazole was detected at 6.9 ppm.

Class IIclassification
F-0017-2018official record ID
Oct 18, 2017report date

Recall record at a glance

Official recordF-0017-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmApple King, LLC
Report dateOct 18, 2017
Recall initiation dateSep 8, 2017
Quantity11,801 cases
LocationYakima, WA, United States

Official product description

Fuji apples, Nature's Delight brand, packaged in tray pack box size 64, net weight 40 lbs., PLU 4131, distributed by L&M Yakima, WA 98903

Why the product was recalled

Fuji apples are recalled because Thiabendazole was detected at 6.9 ppm.

Distribution information

distributed in AL, AZ, CA, CO, FL, GA, HI, ID, IL, IN, IA, MI, MN, NY, OR, SC, TX, WA and in Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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