Square Mile Original Hard Apple Cider is hard cider is in liquid…
Reason Square Mile Original Hard Apple Cider is recalled because bottles may burst.
Square Mile Spur & Vine Hopped Apple Cider is hopped hard cider… recall
Recalled by Craft Brewers Alliance Inc. · Portland, OR, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Square Mile Spur & Vine Hopped Apple Cider is recalled because bottles may burst.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Square Mile Spur & Vine Hopped Apple Cider is hopped hard cider is in liquid form and is an alcoholic beverage. It is packaged in 22 fl oz glass bottles shipped in a corrugated master carton that contains 12 bottles. Individual bottle is sold at retail stores. UPC codes case: 7-02770-04912-0 UPC Bottle: 7-02770-24910-0 PDCN code: CAB12
Quantity: 2699 cases/12 bottles/22 fl oz.
Food: Fresh fruit Juice & beverages
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.
Products packaged on or before May 15, 2013. Individual bottle does not have any codes.
Where it was sold
California Oregon Washington
FDA's distribution note: Distributed in California, Oregon, Washington
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
- Craft Brewers Alliance Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 16, 2013
- In FDA report of
- Aug 21, 2013
- Terminated
- Nov 18, 2013
- FDA recall number
- F-1785-2013 · event 65809
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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