FDA recall record

ConAgra Foods David Trail Mix Sweet & Salty individual plastic bags net wt recall — FDA F-0420-2016

Product contains undeclared milk.

Class Iclassification
F-0420-2016official record ID
Jan 13, 2016report date

Recall record at a glance

Official recordF-0420-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmConAgra Foods Inc.
Report dateJan 13, 2016
Recall initiation dateOct 24, 2015
QuantityUPC 26200-23885 - 299,776 cases; UPC 26200-23890 - 2,803 cases; and UPC 27000-82339 - 200 cases
LocationOmaha, NE, United States

Official product description

David Trail Mix Sweet & Salty individual plastic bags net wt. 5 oz. (142 g) UPC 00 26200 23885 2 shipped in the following configurations: 1) cases of eight (8) with UPC 20-0-26200-23885-6; 2) 36-count multi-pack shipper case UPC 00-0-26200-23890-6 which contains 16 individual 5.25 oz. bags of Classic flavor and 20 individual 5 oz. bags Sweet & Salty flavor UPC 00 26200 23885 2; and 3) 24-count snack rack case UPC 27000-82339 store display which contains individual 5 oz. bags Sweet & Salty flavor UPC 00 26200 23885 2.

Why the product was recalled

Product contains undeclared milk.

Distribution information

Product was distributed nationwide in the United States. Foreign distribution to Hong Kong and Mexico. Product was distributed to military bases in Georgia; no other government distribution.

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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