Prolotherapy with Phenol — Class I drug recall D-1829-2015
Terminated recall by Hartley Medical Center Pharmacy, Incorporated, reported 2015-10-07, distributed in CA, NV. Non-Sterility: Hartley Medical Center Pharmacy, Inc. is recalling Prolotherapy with Phenol due to non-sterilit
| Recall number | D-1829-2015 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hartley Medical Center Pharmacy, Incorporated, Long Beach, CA, United States |
| Recall initiated | 2015-08-17 |
| Classified | 2015-09-25 |
| Reported by FDA | 2015-10-07 |
| Terminated | 2015-12-30 |
| Distributed | CA, NV |
| Quantity | 14 vials |
| Reason classes | sterility |
| Lot numbers | 323132, 328690 |
| Expiration dates | 2015-10-06, 2015-12-01 |
Product
Prolotherapy with Phenol (Dextrose 25%, Glycerin 10%, Lidocaine HCl 10%, Bupivacaine HCl 0.625%, Phenol 1%, QS SWI), 5 mL vial, Rx Only, Hartley Medical, (888) 671-2888
Reason for recall
Non-Sterility: Hartley Medical Center Pharmacy, Inc. is recalling Prolotherapy with Phenol due to non-sterility concerns.
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-1829-2015. 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.