FDA recall record
LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSAS STREET, MEMPHIS, TN 38106, UPC 070596003655
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of May 29, 2015. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSAS STREET, MEMPHIS, TN 38106, UPC 070596003655
Reason
Product has a cloudy appearance
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSAS STREET, MEMPHIS, TN 38106, UPC 070596003655
Code information listed by FDA
MAER , MAES, MAEX, MAFO, MAFA, MAJG, MADB, MAHX, MAGX
Distribution and firm information
Recalling firm listed by FDA: Keystone Laboratories Inc
Firm location listed by FDA: Memphis, TN, United States
Distribution reported by FDA: GA, CT, OR, CA, FL, IL, MD, TN, NJ, NC, Nassau, Bahamas
Product quantity listed by FDA: 39,498 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.