Reported Oct 11, 2023 · Terminated

PHENYLephrine in 0.9% sodium chloride, 1,000 mcg/10 mL, (100 mcg/mL), 10 mL syringe, Rx only, Central Admixture…

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
    • 1
    • 000 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
    • 17-275152
    • 17-275154
    • 17-275155
    • 17-275156
    • 17-275163
    • Exp. 10/1/2023
    • 17-275234
    • 17-275236
    • 17-275251
    • 17-275268
    • 17-275270
    • 17-275277
    • Exp. 10/2/2023
    • 17-275283
    • 17-275294
    • 17-275313
    • Exp. 10/3/2023
    • 17-275469
    • 17-275471
    • 17-275473
    • 17-275480
    • 17-275481
    • 17-275482
    • 17-275483
    • 17-275484
    • 17-275485
    • 17-2754990
    • 17-2754991
    • 17-2754993
    • Exp. 10/4/2023
    • 17-275558
    • 17-275654
    • 17-275667
    • Exp. 10/8/2023
    • 17-275722
    • 17-275737
    • Exp. 10/9/2023
    • 17-275768
    • 17-275804
    • 17-275805
    • Exp. 10/10/2023
    • 17-275847
    • 17-275849
    • 17-275857
    • 17-275882
    • Exp. 10/11/2023
    • 17-275923
    • Exp. 10/12/2023
    • 17-275983
    • 17-275984
    • Exp. 10/15/2023
    • 17-276123
    • Exp. 10/17/2023
    • 17-276125
    • 17-276126
    • Exp. 10/18/2023
Amount recalled
19,510 10 mL syringes.

This recall covers 32 products

The agency filed one notice per product. You are reading one of them; the other 31 are below.

19 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Lack of assurance of sterility:

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 19, 2025 · Data as of Sep 19, 8:09 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.