LONG AID Curl Activator Gel recall
Recalled by Keystone Laboratories Inc · Memphis, TN, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Product has a cloudy appearance
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSAS STREET, MEMPHIS, TN 38106, UPC 070596003655
Quantity: 39,498 units
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.
MAER , MAES, MAEX, MAFO, MAFA, MAJG, MADB, MAHX, MAGX
Where it was sold
California Connecticut Florida Georgia Illinois Maryland North Carolina New Jersey Oregon Tennessee
FDA's distribution note: GA, CT, OR, CA, FL, IL, MD, TN, NJ, NC, Nassau, Bahamas
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
- Keystone Laboratories Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 13, 2013
- In FDA report of
- Nov 5, 2014
- Terminated
- May 29, 2015
- FDA recall number
- F-0080-2015 · event 69311
- Official record
- FDA enforcement report search