D-1833-2015 Class II Terminated
FDA drug recall D-1833-2015 was initiated by Medistat RX L.L.C. on September 10, 2015 and is designated Class II. Reason for recall: Lack of Assurance of Sterility The recall status is terminated (terminated August 30, 2016). Affected quantity: 956,571 mL.
Recall Details
- Product Type
- Drugs
- Report Date
- October 7, 2015
- Initiation Date
- September 10, 2015
- Termination Date
- August 30, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 956,571 mL
Product Description
All Products Intended to be Sterile, mediStat Pharmacy, 110 East Azalea Ave., Foley, AL 36535, 844*737*2550. An Incomplete List of Recalled Products Includes 1) All Cyanacobalamin Products, 2) All Magnesium Chloride Products, 3) All Lipostat (MIC B12) Products, 4) All Trimix (Papaverine/ Aloprostadil/ Phentolamine) Products, 5) All Testosterone Products, 6) All Dexamethasone Products, 7) All Levocarnitine Products, 8) All Hydroxyprogesterone Caproate Products, 9) All Triamcinolone Products, 10) All Betamethasone Sodium Phosphate Products, 11) All Methylprednisolone Acetate Products.
Reason for Recall
Lack of Assurance of Sterility
Distribution Pattern
U.S. Nationwide
Code Information
All Lots Not Expired and Distributed Before 8/5/15.