Diltiazem HCl 125 mg in 5% Dextrose 125 mL Single-Dose- Bag — Class II drug recall D-1073-2017
Terminated recall by Cantrell Drug Company, reported 2017-08-16, distributed nationwide. Lack of Sterility Assurance.
| Recall number | D-1073-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cantrell Drug Company, Little Rock, AR, United States |
| Recall initiated | 2017-07-14 |
| Classified | 2017-08-09 |
| Reported by FDA | 2017-08-16 |
| Terminated | 2020-09-16 |
| Distributed | Nationwide (US) |
| Quantity | 2,761 bags |
| Reason classes | sterility |
| NDC | 52533-0103-13 |
| Lot numbers | 10084, 10137, 10252, 10271, 10350, 10491 |
| Expiration dates | 2017-07-25, 2017-08-02, 2017-08-15, 2017-08-17, 2017-08-30, 2017-09-21 |
Product
Diltiazem HCl 125 mg in 5% Dextrose 125 mL Single-Dose- Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222; NDC 52533-103-13
Reason for recall
Lack of Sterility Assurance.
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-1073-2017. 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.