Dexpanthenol 250 mg/mL PF — Class II drug recall D-1035-2013
Terminated recall by Wellness Pharmacy, Inc., reported 2013-09-18, distributed nationwide. Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results indicating micro
| Recall number | D-1035-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wellness Pharmacy, Inc., Birmingham, AL, United States |
| Recall initiated | 2013-08-23 |
| Classified | 2013-09-12 |
| Reported by FDA | 2013-09-18 |
| Terminated | 2014-06-03 |
| Distributed | Nationwide (US) |
| Quantity | 1,355 vials |
| Reason classes | microbial contamination, sterility |
| Expiration dates | 2013-12-02 |
Product
Dexpanthenol 250 mg/mL PF, Single Use Vial, 1 mL, WELLNESS PHARMACY, 1-800-227-2627
Reason for recall
Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable.
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-1035-2013. 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.