Severity
Low
LowClass IIITerminated
FDA Food recall · Reported November 5, 2014
LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSAS STREET, MEMPHIS, TN 38106, UPC 070596003655
Product has a cloudy appearance
Keystone Laboratories Inc recalled LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSA… - a low-severity action.
LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSA… was recalled by Keystone Laboratories Inc in November 5, 2014. Reason: Product has a cloudy appearance. Check the official notice for the remedy. Verify recall #F-0080-2015 with the FDA Food before acting.
The recall
Keystone Laboratories Inc issued this low-severity FDA Food recall-Product has a cloudy appearance.
- Low
- severity level
- 39K units
- affected scope
- Class III
- classification
- November 5, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0080-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0080-2015) was formally reported on November 5, 2014, with the manufacturer initiating the action on December 13, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Keystone Laboratories Inc is listed as the recalling firm, operating out of Memphis, TN. Federal records list the affected scope as 39,498 units.
The documented reason for this recall is: Product has a cloudy appearance Distribution data in the federal record shows the product reached: GA, CT, OR, CA, FL, IL, MD, TN, NJ, NC, Nassau, Bahamas. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
39,498 units
Related Recalls
6
2 from same agency
Product description
LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSAS STREET, MEMPHIS, TN 38106, UPC 070596003655
Reason for recall
Product has a cloudy appearance
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0080-2015 |
| Date reported | November 5, 2014 |
| Date initiated | December 13, 2013 |
| Recalling firm | Keystone Laboratories Inc |
| Firm location | Memphis, TN |
| Affected scope | 39,498 units |
| Distribution | GA, CT, OR, CA, FL, IL, MD, TN, NJ, NC, Nassau, Bahamas |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0080-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSAS STREET, MEMPHIS, TN 38106, UPC 070596003655. Recalled by Keystone Laboratories Inc. Units affected: 39,498 units.
Why was this product recalled? ▼
Product has a cloudy appearance
Which agency issued this recall? ▼
This recall was issued by the FDA Food on November 5, 2014. Severity: Low. Recall number: F-0080-2015.
Where was the recalled product distributed? ▼
Distribution: GA, CT, OR, CA, FL, IL, MD, TN, NJ, NC, Nassau, Bahamas.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0080-2015) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported November 5, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.