FDA recall record

Newman's Own Organics brand Newman-O's Peanut Butter Creme recall — FDA F-0292-2013

The product was manufactured using peanut butter recalled by Sunland Inc. and it may be contaminated with Salmonella.

Class Iclassification
F-0292-2013official record ID
Oct 24, 2012report date

Recall record at a glance

Official recordF-0292-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmNewman's Own Organics
Report dateOct 24, 2012
Recall initiation dateSep 27, 2012
Quantity4,609 cases or 27,654 packages total; With expansion: 146,213 cases
LocationAptos, CA, United States

Official product description

Newman's Own Organics brand Newman-O's Peanut Butter Creme Filled Chocolate Cookies 8oz/6 pack, Unit UPC#7 57645 02170 8, Case UPC#7 57645 02171 5; 13oz/6 pack, Unit UPC# 7 57645 02150 0, Case UPC#7 57645 02151 7; 9oz/6 pack, Unit UPC#7 57645 02288 0, Case UPC # 7 57645 02388 7; 16oz/ 12 pack, Unit UPC# 7 57645 02239 2, Case UPC # 7 57645 02339 9; Product is manufactured by J&J Snack Foods, 5353 Downey Rd., Vernon, CA and distributed by Newman's Own Organics, Aptos, CA

Why the product was recalled

The product was manufactured using peanut butter recalled by Sunland Inc. and it may be contaminated with Salmonella.

Distribution information

The product is distributed in the US only. Firm's distributors are location nationwide: AZ, CA, CO, CT, GA, NH, IA, IL, IN, NJ, NV, OR, PA, TN, TX, WA. However, the firm's distributors service a large area and can ship to retailers outside of their state.

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: E-Mail.

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.

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