Food, drugs, devices › InvaGen Pharmaceuticals, Inc.
Drug recall: Decitabine for Injection, 50mg per vial, Rx only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla
FDA enforcement event 79729 is a drug recall by InvaGen Pharmaceuticals, Inc. of Central Islip, NY, initiated 5 Mar 2018 and classified Class III, with 1 product record.
FDA defines Class III as a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences. 29% of the 367 drug enforcement events initiated in 2018 carry the same class.
Status: Terminated, terminated 20 Jan 2021. Initiation: voluntary: firm initiated. InvaGen Pharmaceuticals, Inc. has 8 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
InvaGen Pharmaceuticals, Inc., Central Islip, NY.
Reason for recall
"Failed impurities/degradation specifications: Failure to water content and impurity"
Distribution
"U.S.A. nationwide"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| D-0698-2018 | Decitabine for Injection, 50mg per vial, Rx only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla USA, Inc., 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise, FL 33323, NDC 69097-285-37 | 3222 vials | Class III | Terminated | 18 Apr 2018 |
Context
Other enforcement events for InvaGen Pharmaceuticals, Inc.
All 8 events for InvaGen Pharmaceuticals, Inc.
Questions and answers
Why was this drug recalled?
FDA's record gives the reason for recall as: "Failed impurities/degradation specifications: Failure to water content and impurity"
What does Class III mean?
FDA classifies recalls by relative degree of health hazard. Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
Where was the product distributed?
FDA's distribution pattern field reads: "U.S.A. nationwide"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 20 Jan 2021. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA drug enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.