Food Recall Check
Class I · High risk Terminated Initiated Jun 14, 2016 (10 years ago)

molly&drew The Beer Bread Company recall

Recalled by Big L Brands Inc DBA molly&drew The Beer Bread Company · Sac City, IA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

The product contains an ingredient that is being recalled by the ingredient supplier. The ingredient is potentially contaminated with E. coli O121. Recall was started on 6/14/16.

Pathogen: E. coli

Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

molly&drew The Beer Bread Company, Beer Bread Mix, NET WT. 19.75 OZ, UPC 8 55290 00300 8, molly & drew Sac City, IA. Packed in paper bags.

Quantity: 6000 bags

Food: Bread & bakery

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot # L1215A, L1215B, L1215C, BEST BY:01/2018

Where it was sold

Tennessee

FDA's distribution note: Product was distributed one consignee in Tennessee

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Big L Brands Inc DBA molly&drew The Beer Bread Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 14, 2016
In FDA report of
Sep 21, 2016
Terminated
Sep 11, 2018
FDA recall number
F-2202-2016 · event 74411
Official record
FDA enforcement report search

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