D-1032-2019 Class II Terminated
FDA drug recall D-1032-2019 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: 1850 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
- 1850 syringes
Product Description
Phenylephrine HCl, 1 mg in Sterile Water for Injection, QS 10 mL Injectable Solution 1 mg/10 mL (100 mcg per mL) NDC: 42852-802-61 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: 11/01/18 8847 80261S Exp. 3/31/2019