FDA recall record

Wawona Packing Company Sweet 2 Eat Yellow Peaches recall — FDA F-0616-2015

Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be…

Class Iclassification
F-0616-2015official record ID
Dec 17, 2014report date

Recall record at a glance

Official recordF-0616-2015
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmWawona Packing Company
Report dateDec 17, 2014
Recall initiation dateJul 18, 2014
Quantity2.2 millions boxes (20 lbs per box) estimated since 6-2014
LocationCutler, CA, United States

Official product description

Sweet 2 Eat Yellow Peaches; California Tree Fruit; Product of USA; Packed in the following configurations: 2.5 lb. box, 4-4.5 lb. box 4-4.5 lb box for Trader Joe's 8/2 Clamshell - net weight 2 lbs. Costco Consumer Box, 5 lbs Sam's Club consumer box - 4 lbs (Summer Flame) BJ's 4 lb clamshell 2 lb bag. Sticker information - Sweet 2 Eat: 94044 Org TR YF Peach 4044 TR Peach; 4038 CA Peach Varieties include: August Flame, August Lady, , Autumn Flame, Bright Princess, Brittney Lane, Candy Flame, Crimson Lady, Crimson Princess, Earli Rich, Elegant Lady, Grand Finale, Henry 2,3 & 4, July Flame, June Flame, June Flavor, June Time, Kaweah, King Midas 17, Last Tango., May Princess, O'Henry, , Princess Time, Rich Lady,, Sierra Rich, Spring Flame 18, 20, 20.5, 21, 22, SU Peach 13, 15, 17, Sugartime, Summer Flame 26, 29. 24, , Summer Zee, Sweet Dream, Sweet Henry, Tra Zee, Vista, Zee Lady, Zee Pride. Wawona Packing Cutler, CA.

Why the product was recalled

Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.

Distribution information

Worldwide distribution including Canada, Taiwan, Singapore, Indonesia, Malaysia, Columbia, Costa Rica, Guatemala, Honduras, Australia, India, Mexico, Philippines, Brazil, Hong Kong, Ecuador and Manila

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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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