FDA Drug Recalls

Recalls / Class III

Class IIID-0497-2019

Product

Oxytocin 10 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1001 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-730-99.

Affected lot / code info
Lot: 12/20/18 1056 73099P, BUD: 02/03/2019

Why it was recalled

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

Recalling firm

Firm
Advanced Pharma Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
9265 Kirby Dr, Houston, Texas 77054-2520

Distribution

Quantity
12 bags
Distribution pattern
Nationwide in the USA.

Timeline

Recall initiated
2019-02-06
FDA classified
2019-02-15
Posted by FDA
2019-02-27
Terminated
2019-10-30
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0497-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class III recall: drug · FDA Drug Recalls