Drug recall
Cefazolin for Injection, USP, 1 gram, packaged in packs of 25/1 gram vials, Rx only, For I.M. or I.V. use…
FDA recall event 52432 · Class II · Sandoz, Inc
Key facts
| Event ID | 52432 |
|---|---|
| Recall numbers | D-1881-2009 |
| Recalling firm | Sandoz, Inc |
| Product type | Drugs |
| Products | Cefazolin for Injection, USP, 1 gram, packaged in packs of 25/1 gram vials, Rx only, For I.M. or I.V. use, Sterile, Manufactured in Austria by Sandoz GmbH for Sandoz Inc., Princeton, NJ. --- NDC… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Misbranded; product carton incorrectly states reconstitute with 2mL sterile water but should correctly state reconstitute with 2.5mL sterile water. Both immediate vial label and insert are correct. |
| Initiation date | Jun 12, 2009 |
| Termination date | Mar 9, 2010 |
| City | Princeton |
| State | NJ |
| Country | United States |
| FEI number | 3006697677 |
At a glance
- 1–9 Products in this recall
- None 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