Paricalcitol Capsules — Class III drug recall D-0721-2016
Terminated recall by Dr. Reddy's Laboratories, Inc., reported 2016-02-24, distributed nationwide. Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol
| Recall number | D-0721-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dr. Reddy's Laboratories, Inc., Princeton, NJ, United States |
| Recall initiated | 2015-11-04 |
| Classified | 2016-02-18 |
| Reported by FDA | 2016-02-24 |
| Terminated | 2017-06-22 |
| Distributed | Nationwide (US) |
| Quantity | 11,123 bottles |
| Reason classes | packaging, device malfunction |
| NDC | 55111-0663, 55111-0663-01, 55111-0663-05, 55111-0663-30, 55111-0663-79, 55111-0663-81, 55111-0664, 55111-0664-01, 55111-0664-05, 55111-0664-30, 55111-0664-79, 55111-0664-81, 55111-0665, 55111-0665-01, 55111-0665-05, 55111-0665-30, 55111-0665-79, 55111-0665-81 |
| Lot numbers | C404440, C404946, C505704 |
| Expiration dates | 2016-04, 2016-05, 2017-07 |
Product
Paricalcitol Capsules, 4 mcg, 30 capsules per bottle, Rx Only, Mfd by: Dr. Reddy's Laboratories Limited, Bachupally, India, NDC 55111-665-30
Reason for recall
Failed Tablet/Capsule Specifications: Product recalled due to reports of breakage and leakage of Paricalcitol capsules.
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-0721-2016. 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.