Data Foundry

Drug recalls 2019

Oxytocin 30 Units added to NS 500 mL — Class III drug recall D-0499-2019

Terminated recall by Advanced Pharma Inc., reported 2019-02-27, distributed nationwide. Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.

Recall numberD-0499-2019
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAdvanced Pharma Inc., Houston, TX, United States
Recall initiated2019-02-06
Classified2019-02-15
Reported by FDA2019-02-27
Terminated2019-10-30
DistributedNationwide (US)
Quantity1,460 bottles
Reason classeslabeling, potency
NDC42852-0706-50
Lot numbers3177, 5698, 6618, 70650P, 7716
Expiration dates2019-02-10, 2019-02-12, 2019-03-16

Product

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0499-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.