Reported Aug 9, 2023 · Terminated

PHENYLephrine in 0.9% sodium chloride, 1000 mcg/10 mL, (100 mcg/mL), 10 mL syringe, Rx only, Central Admixture Pharmacy…

Central Admixture Pharmacy Services Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Central Admixture Pharmacy Services Inc · 7935 Dunbrook Rd Ste C · San Diego, CA · 92126-6322

Is this the product you have?

  • PHENYLephrine in 0.9% sodium chloride, 1000 mcg/10 mL, (100 mcg/mL), 10 mL syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-6009-1
Lot codes and dates
  • Lot

    211 of 211 codes

    • 17-270449
    • 17-270450
    • 17-270453
    • 17-270462
    • 17-270465
    • 17-270466
    • 17-270494
    • 17-270495
    • 17-270502
    • 17-270541
    • Exp. 7/16/2023
    • 17-270582
    • 17-270585
    • 17-270587
    • 17-270592
    • 17-270593
    • 17-270598
    • 17-270610
    • 17-270611
    • 17-270612
    • Exp. 7/17/2023
    • 17-270900
    • 17-270902
    • 17-270906
    • 17-270907
    • 17-270908
    • 17-270909
    • 17-270953
    • 17-270955
    • 17-270991
    • 17-270993
    • Exp. 7/23/2023
    • 17-271047
    • 17-271048
    • 17-271050
    • 17-271053
    • Exp. 7/24/2023
    • 17-271344
    • 17-271349
    • 17-271355
    • 17-271356
    • 17-271405
    • 17-271406
    • Exp. 7/31/2023
    • 17-271478
    • 17-271479
    • 17-271480
    • 17-271484
    • 17-271495
    • 17-271500
    • Exp. 7/31/2023
    • 17-271744
    • 17-271763
    • Exp. 8/3/2023
    • 17-271838
    • 17-271851
    • Exp. 8/6/2023
    • 17-271871
    • 17-271873
    • 17-271886
Amount recalled
81,073 syringes

This recall covers 39 products

The agency filed one notice per product. You are reading one of them; the other 38 are below.

26 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Mar 21, 2025 · Data as of Sep 19, 8:08 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.