D-0499-2019 Class III Terminated

Recalled by Advanced Pharma Inc. — Houston, TX

FDA drug recall D-0499-2019 was initiated by Advanced Pharma Inc. on February 6, 2019 and is designated Class III. Reason for recall: Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label. The recall status is terminated (terminated October 30, 2019). Affected quantity: 1460 bottles.

Recall Details

Product Type
Drugs
Report Date
February 27, 2019
Initiation Date
February 6, 2019
Termination Date
October 30, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1460 bottles

Product Description

Oxytocin 30 Units added to NS 500 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 503 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-706-50.

Reason for Recall

Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.

Distribution Pattern

Nationwide in the USA.

Code Information

Lots: 11/27/18 3177 70650P, BUD: 02/10/2019; 11/27/18 6618 70650P, BUD: 02/10/2019; 11/28/18 7716 70650P, BUD: 02/12/19; 12/31/18 5698 70650P, BUD: 03/16/19