Drug recall

Chocolate Peanut Butter Bundts are sold by individual slices through cafe display case counters with a food…

FDA recall event 51123 · Class I · Allan Brothers Coffee Llc

Key facts

Event ID 51123
Recall numbers F-300-9, F-301-9, F-302-9, F-303-9, F-304-9, F-305-9, F-306-9, F-307-9, F-308-9, F-309-9, F-310-9, F-311-9 and 4 more
Recalling firm Allan Brothers Coffee Llc
Product type Food
Products Chocolate Peanut Butter Bundts are sold by individual slices through cafe display case counters with a food card identifying the name of the product. No UPC codes, or labels, exist for this product., Chocolate Peanut Butter Cake is sold by individual slices through cafe display case counters with a food card identifying the name of the product. No UPC codes, or labels, exist for this product., Cowboy Cookies are sold by individual cookie through cafe display case counters with a food card identifying the name of the product. No UPC codes, or labels, exist for this product., Double Delicious Bars are sold by individual bars through cafe display case counters with a food card identifying the name of the product. No UPC codes, or labels, exist for this product., Monster Cookies are sold by individual cookie through cafe display case counters with a food card identifying the name of the product. No UPC codes, or labels, exist for this product. and 11 more
Classification Class I
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall The product was manufactured using peanuts recalled by Peanut Corporation of America because they gave the potential to be contaminated with Salmonella., The product was manufactured using peanuts recalled by Peanut Corporation of America because they have the potential to be contaminated with Salmonella.
Initiation date Feb 5, 2009
Termination date Jul 20, 2009
City Albany
State OR
Country United States
FEI number 3003265442

At a glance

  • 10–99 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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