CLASS III Drug recall · Reported 31 Dec 2014 · FDA Enforcement Report

sulfur8(R) medicated anti-dandruff conditioner recalled

J. Strickland is recalling sulfur8(R) medicated anti-dandruff conditioner, dandruff treatment for Braids, spray, distributed nationwide in the US. The recall was initiated on 9 Dec 2014 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot number: 13TG
Quantity recalled1506 (case of 12)

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0318-2015
FDA event ID
69977
Recalling firm
J. Strickland, Olive Branch, MS
Classification
Class III
Status
Terminated
Recall initiated
9 Dec 2014
FDA classified
23 Dec 2014
Reported
31 Dec 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

9 Dec 2014Recall initiated by company
23 Dec 2014Classified by FDA+14 days
31 Dec 2014Published in enforcement report+8 days

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

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.

Product as listed by the FDA

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

Where it was distributed

Nationwide and International: Bahamas and Jamaica

Nationwide

Questions about this recall

Why was it recalled?

Failed pH specification: Product pH test value of 5.72 failed to meet its product specification of 6.0 to 7.5.

Which lots are affected?

Lot number: 13TG

Where was it sold?

Nationwide and International: Bahamas and Jamaica

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

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 26 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 J. Strickland

All 2
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIIsulfur8 medicated Light Formula recalled by J. Strickland andJ. StricklandPotency & AssayNationwide