Drug recall D-0145-2017
Product
Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH for Hospira Worldwide, Inc., Lake Forest, Il 60045, USA, Made in Austria, NDC 0409-7332-01
Reason for recall
Labeling: Missing Label
Lots and codes
Sandoz - Lot GJ7151(Pfizer- Lot 670028M); Exp. 07/19
Recall details
- Recalling firm
- Sandoz Inc, Princeton, NJ
- Quantity
- 139,430 vials
- Distribution
- WI
- Type
- Voluntary: Firm initiated
- Recall initiated
- October 19, 2016
- Terminated
- July 27, 2017
Related products
- Ceftriaxone Sodium – drug information
- NDC 0409-7338 Ceftriaxone Sodium · Ceftriaxone Sodium 500 mg/1 · Hospira, Inc
- NDC 0409-7332 Ceftriaxone Sodium · Ceftriaxone Sodium 1 g/1 · Hospira, Inc
- NDC 0409-7337 Ceftriaxone Sodium · Ceftriaxone Sodium 250 mg/1 · Hospira, Inc
- NDC 0409-7335 Ceftriaxone Sodium · Ceftriaxone Sodium 2 g/1 · Hospira, Inc