McCafe Premium Roast Decaf Coffee K-Cup Pods
Reason Product is labeled as decaf, but might contain caffeine.
Rc Cola recall
Recalled by Keurig Dr Pepper · Frisco, TX, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Consumer complaints of off flavor and aroma
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack
Quantity: 9238 cases
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.
production code of the product is G1211 CB3U
Where it was sold
Georgia Indiana Kentucky New Jersey Ohio Pennsylvania Tennessee Virginia West Virginia
FDA's distribution note: West Virginia, Virginia, Ohio, Kentucky, Indiana, Pennsylvania, New Jersey, Tennessee, Georgia.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Keurig Dr Pepper
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 13, 2021
- In FDA report of
- Oct 6, 2021
- Terminated
- Dec 8, 2021
- FDA recall number
- F-0008-2022 · event 88723
- Official record
- FDA enforcement report search
Other recalls by Keurig Dr Pepper
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods
Reason Product contains black tea, resulting in caffeine being undeclared.
Diet Snapple Tea Peach Tea
Reason Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.
Target Good & Gather Mixed Berry Sparkling Water
Reason The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained unlabeled sulfites.