Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported December 31, 2014
sulfur8(R) medicated anti-dandruff conditioner, dandruff treatment for Braids, spray, Active Ingredient: Salicylic Acid, 2%, 12 FL OZ (356ml) spray bottle, OTC, Made in the U.S.A. J. Strickland & Co., OLIVE BRANCH, MS 38654 UPC: 0 7561044510 7
Failed pH specification: Product pH test value of 5.72 failed to meet its product specification of 6.0 to 7.5.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
J. Strickland and Co recalled sulfur8(R) medicated anti-dandruff conditioner, dandruff treatment for Braids, spray, Ac… - a low-severity action.
sulfur8(R) medicated anti-dandruff conditioner, dandruff treatment for Braids, spray, Ac… was recalled by J. Strickland and Co in December 31, 2014. Reason: Failed pH specification: Product pH test value of 5.72 failed to meet its product specification of 6.0 to 7.5.. Check the official notice for the remedy. Verify recall #D-0318-2015 with the FDA Drug before acting.
The recall
J. Strickland and Co issued this low-severity FDA Drug recall-Failed pH specification: Product pH test value of 5.72 failed to meet its product specification of 6.0 to 7.5..
- Low
- severity level
- Class III
- classification
- December 31, 2014
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0318-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0318-2015) was formally reported on December 31, 2014, with the manufacturer initiating the action on December 9, 2014. It is classified under Low severity (Class III), with a current status of Terminated. J. Strickland and Co is listed as the recalling firm, operating out of Olive Branch, MS. Federal records list the affected scope as 1506 (case of 12).
The documented reason for this recall is: Failed pH specification: Product pH test value of 5.72 failed to meet its product specification of 6.0 to 7.5. Distribution data in the federal record shows the product reached: Nationwide and International: Bahamas and Jamaica. 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 - 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products 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
1506 (case of 12)
Related Recalls
6
0 from same agency
Product description
sulfur8(R) medicated anti-dandruff conditioner, dandruff treatment for Braids, spray, Active Ingredient: Salicylic Acid, 2%, 12 FL OZ (356ml) spray bottle, OTC, Made in the U.S.A. J. Strickland & Co., OLIVE BRANCH, MS 38654 UPC: 0 7561044510 7
Reason for recall
Failed pH specification: Product pH test value of 5.72 failed to meet its product specification of 6.0 to 7.5.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0318-2015 |
| Date reported | December 31, 2014 |
| Date initiated | December 9, 2014 |
| Recalling firm | J. Strickland and Co |
| Firm location | Olive Branch, MS |
| Affected scope | 1506 (case of 12) |
| Distribution | Nationwide and International: Bahamas and Jamaica |
Profile values are sourced directly from the official FDA Drug 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 (D-0318-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug 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 Drug 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? ▼
sulfur8(R) medicated anti-dandruff conditioner, dandruff treatment for Braids, spray, Active Ingredient: Salicylic Acid, 2%, 12 FL OZ (356ml) spray bottle, OTC, Made in the U.S.A. J. Strickland & Co., OLIVE BRANCH, MS 38654 UPC: 0 7561044510 7. Recalled by J. Strickland and Co. Units affected: 1506 (case of 12).
Why was this product recalled? ▼
Failed pH specification: Product pH test value of 5.72 failed to meet its product specification of 6.0 to 7.5.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 31, 2014. Severity: Low. Recall number: D-0318-2015.
Where was the recalled product distributed? ▼
Distribution: Nationwide and International: Bahamas and Jamaica.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0318-2015) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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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 Drug, reported December 31, 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.