Drug recall
Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL vial, For Intramuscular Use Only, Rx Only…
FDA recall event 76742 · Class II · Sun Pharmaceutical Industries, Inc.
Key facts
| Event ID | 76742 |
|---|---|
| Recall numbers | D-0611-2017 |
| Recalling firm | Sun Pharmaceutical Industries, Inc. |
| Product type | Drugs |
| Products | Testosterone Cypionate Injection , USP, 200 mg/mL, 1 mL vial , For Intramuscular Use Only, Rx Only, Distributed by Sun Pharma Ind. Inc., NJ 08512, Manufactured by Sun Pharma Ind. Ltd. India, NDC… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Presence of Particulate Matter |
| Initiation date | Mar 15, 2017 |
| Report date | Mar 29, 2017 |
| Termination date | Apr 23, 2018 |
| City | Cranbury |
| State | NJ |
| Country | United States |
| FEI number | 3005551493 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: