CLASS III Food recall · Reported 5 Nov 2014 · FDA Enforcement Report

LONG AID Curl Activator Gel recalled by Keystone Laboratories

Keystone Laboratories is recalling LONG AID Curl Activator Gel, distributed in 10 states. The recall was initiated on 13 Dec 2013 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesMAER , MAES, MAEX, MAFO, MAFA, MAJG, MADB, MAHX, MAGX
Quantity recalled39,498 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0080-2015
FDA event ID
69311
Recalling firm
Keystone Laboratories, Memphis, TN
Classification
Class III
Status
Terminated
Recall initiated
13 Dec 2013
FDA classified
24 Oct 2014
Reported
5 Nov 2014
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Other Reasons
Product category
Other

Timeline

13 Dec 2013Recall initiated by company
24 Oct 2014Classified by FDA+315 days
5 Nov 2014Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product has a cloudy appearance

Product as listed by the FDA

LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSAS STREET, MEMPHIS, TN 38106, UPC 070596003655

Where it was distributed

GA, CT, OR, CA, FL, IL, MD, TN, NJ, NC, Nassau, Bahamas

CaliforniaConnecticutFloridaGeorgiaIllinoisMarylandNorth CarolinaNew JerseyOregonTennessee

Questions about this recall

Is LONG AID Curl Activator Gel recalled?

Yes. Keystone Laboratories recalled LONG AID Curl Activator Gel on 13 Dec 2013. The recall is Class III and its status is Terminated. Recall number F-0080-2015.

Why was it recalled?

Product has a cloudy appearance

Which lots are affected?

MAER , MAES, MAEX, MAFO, MAFA, MAJG, MADB, MAHX, MAGX

Where was it sold?

GA, CT, OR, CA, FL, IL, MD, TN, NJ, NC, Nassau, Bahamas

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Keystone Laboratories

All 3

Other Other recalls

All 4,664