D-1031-2019 Class II Terminated
FDA drug recall D-1031-2019 was initiated by Advanced Pharma Inc. on March 13, 2019 and is designated Class II. Reason for recall: Lack of Assurance of Sterility The recall status is terminated (terminated January 14, 2020). Affected quantity: 1440 syringes.
Recall Details
- Product Type
- Drugs
- Report Date
- March 27, 2019
- Initiation Date
- March 13, 2019
- Termination Date
- January 14, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1440 syringes
Product Description
Heparin 5,000 Units/5mL (1,000 Units per mL) Injectable Solution, 5,000 Units in 0.9% Sodium Chloride, QS 5 mL Sterile single use syringe, NDC: 42852-739-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Reason for Recall
Lack of Assurance of Sterility
Distribution Pattern
Nationwide
Code Information
Lot: 10/25/18 4819 73967S Exp. 3/24/2019