D-0187-2017 Class II Terminated
FDA drug recall D-0187-2017 was initiated by Cantrell Drug Company on November 18, 2016 and is designated Class II. Reason for recall: Lack of Assurance of Sterility - the firm is recalling select sterile drug products. The recall status is terminated (terminated April 29, 2020). Affected quantity: 645 vials.
Recall Details
- Product Type
- Drugs
- Report Date
- December 21, 2016
- Initiation Date
- November 18, 2016
- Termination Date
- April 29, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 645 vials
Product Description
Calcium Chloride, (1 g/10 mL) Injection Solution 10 mL, 10% Single-Dose Vial, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207
Reason for Recall
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Distribution Pattern
Nationwide
Code Information
Lot: 169924