Extra Strength Naturally HL Hemorrhoid Numbing with Lidocaine — Class II drug recall D-0090-2018
Terminated recall by Ridge Properties, LLC, reported 2017-11-29. GMP Deviations: inadequate manufacturing control processes
| Recall number | D-0090-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ridge Properties, LLC, Salem, OR, United States |
| Recall initiated | 2017-11-03 |
| Classified | 2017-11-21 |
| Reported by FDA | 2017-11-29 |
| Terminated | 2019-01-14 |
| Reason classes | cgmp |
| NDC | 69804-0014-03, 69804-0014-06 |
| Expiration dates | 2018-10-17 |
Product
Extra Strength Naturally HL Hemorrhoid Numbing with Lidocaine, (lidocaine HCL 4%), 1/2 oz Balm (NDC 69804-014-06), and 2 oz Balm(NDC 69804-014-03), Manufactured by Pain Relief Naturally, www.Naturally HL.com
Reason for recall
GMP Deviations: inadequate manufacturing control processes
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-0090-2018. 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.