BETTER BRAIDS UN-BRAID — Class II drug recall D-0853-2016
Terminated recall by Keystone Laboratories Inc, reported 2016-05-25, distributed in MD, NJ. Microbial Contamination of Non-Sterile Products: Failed S.aureus test.
| Recall number | D-0853-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Keystone Laboratories Inc, Memphis, TN, United States |
| Recall initiated | 2016-04-04 |
| Classified | 2016-05-16 |
| Reported by FDA | 2016-05-25 |
| Terminated | 2016-05-25 |
| Distributed | MD, NJ |
| Reason classes | microbial contamination, sterility |
| Pathogens | staphylococcus |
| Lot numbers | 10AN5 |
Product
BETTER BRAIDS UN-BRAID (salicylic acid), Le Demelant, Packaged in 12 FL. OZ. (355 ml) Bottles, Over the Counter Only. Distributed by KEYSTONE LABORATORIES, UPC 07059600430.
Reason for recall
Microbial Contamination of Non-Sterile Products: Failed S.aureus test.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0853-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.