D-0064-2016 Class II Terminated
FDA drug recall D-0064-2016 was initiated by JD & SN Inc., dba Moses Lake Professional Pharmacy on July 24, 2015 and is designated Class II. Reason for recall: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry The recall status is terminated (terminated April 13, 2016). Affected quantity: 9 (4mL), 4 (5mL) vials, 9 (6mL) vials, 5 (7.5mL) vials, 4 (10mL) vials, 5 (9mL) vials, 3 (12mL) vials, 2 (15mL) vials, 1.
Recall Details
- Product Type
- Drugs
- Report Date
- November 4, 2015
- Initiation Date
- July 24, 2015
- Termination Date
- April 13, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9 (4mL), 4 (5mL) vials, 9 (6mL) vials, 5 (7.5mL) vials, 4 (10mL) vials, 5 (9mL) vials, 3 (12mL) vials, 2 (15mL) vials, 1 (20mL), 1 (28mL) vials
Product Description
CHORIONIC GONADOTROPIN, Injectable Solution, 200 UNITS/0.1 ML, vial sizes: 4 mL; 5 mL; 6 mL; 7.5 mL ; 9 mL, 10 mL; 12 mL; 15 mL; 20 mL; 28 mL; Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Reason for Recall
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Distribution Pattern
Nationwide
Code Information
11032014@10, 12082014@3, t01082015@26, t03092015@26, t03132015@13, t03162015@12, t03242015@19, t04092015@21, t05132015@28, t05132015@44, t05202015@22, t05262015@14, t05272015@36, t06172015@27, t06182015@7, t06242015@9, t06292015@11, t07092015@42, t07102015@25, t08012014@1, t09122014@19, t09252014@4, t12242014@2, and t12312014@8.