D-1252-2014 Class I Terminated
FDA drug recall D-1252-2014 was initiated by Brookfield Prescription Center Inc on November 13, 2013 and is designated Class I. Reason for recall: Non-Sterility: One lot of Glycopyrrolate solution for injection was found to be contaminated with Bacillus thuringiensis. The recall status is terminated (terminated May 30, 2014). Affected quantity: 25 Vials.
Recall Details
- Product Type
- Drugs
- Report Date
- April 30, 2014
- Initiation Date
- November 13, 2013
- Termination Date
- May 30, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 25 Vials
Product Description
Glycopyrrolate (MDV) 0.2 MG/ML Injectable, 5 mL Vials, Sterile Serum Vials/Sterile Syringes, for use by a licensed professional only, not for resale, MD Custom Rx, 19035 W Capitol Dr Ste 105, Brookfield, WI 53045.
Reason for Recall
Non-Sterility: One lot of Glycopyrrolate solution for injection was found to be contaminated with Bacillus thuringiensis.
Distribution Pattern
WI
Code Information
Lot #: 10292013@15, Beyond Use Date: 11/28/2013