Data Foundry

Drug recalls 2023

PHENYLephrine in 0 — Class II drug recall D-1078-2023

Terminated recall by Central Admixture Pharmacy Services Inc, reported 2023-08-09, distributed nationwide. Lack of assurance of sterility: Lack of validation data for sanitization cycles

Recall numberD-1078-2023
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCentral Admixture Pharmacy Services Inc, San Diego, CA, United States
Recall initiated2023-07-17
Classified2023-08-03
Reported by FDA2023-08-09
Terminated2025-03-21
DistributedNationwide (US)
Quantity16,971 syringes
Reason classessterility
NDC71286-6007-01
Lot numbers17-270510, 17-270512, 17-270665, 17-270699, 17-270812, 17-271062, 17-271063, 17-271064, 17-271065, 17-271350, 17-271357, 17-271421, 17-271422, 17-271836, 17-271848, 17-271890, 17-271943, 17-271954, 17-271958, 17-271962, 17-272162, 17-272174, 17-272175, 17-272176, 17-272177, 17-272444, 17-272456, 17-272473, 17-272717, 17-272721, 17-272732, 17-273550, 17-273565, 17-273579, 17-273580
Expiration dates2023-07-16, 2023-07-18, 2023-07-19, 2023-07-24, 2023-07-30, 2023-08-06, 2023-08-07, 2023-08-08, 2023-08-13, 2023-08-16, 2023-08-21, 2023-09-05

Product

PHENYLephrine in 0.9 sodium chloride, 400 mcg /10 mL, (40 mcg/mL), 10 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6007-1

Reason for recall

Lack of assurance of sterility: Lack of validation data for sanitization cycles

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-1078-2023. 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.