D-1182-2015 Class II Terminated
FDA drug recall D-1182-2015 was initiated by Lincare, Inc. on May 28, 2015 and is designated Class II. Reason for recall: Lack of Assurance of Sterility: Sterility of product is not assured. The recall status is terminated (terminated February 16, 2017). Affected quantity: Unknown.
Recall Details
- Product Type
- Drugs
- Report Date
- July 8, 2015
- Initiation Date
- May 28, 2015
- Termination Date
- February 16, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- Unknown
Product Description
VANC 50MCG/ML-HEP 100U/ML in 2ML, Packed in 2 mL Units, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
Reason for Recall
Lack of Assurance of Sterility: Sterility of product is not assured.
Distribution Pattern
United States including: Arkansas
Code Information
Compounded on 05/27/2015, Discard After: 06/11/2015