Reported Aug 9, 2023 · Terminated

PHENYLephrine 1,000 mcg/10mL, (100mcg/mL) in 0.9% sodium chloride, Syringe, Rx Only, CAPS, Inc., 2200 South 43rd…

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. · 2200 S 43rd Ave · Phoenix, AZ · 85043-3909

Is this the product you have?

  • PHENYLephrine 1,000 mcg/10mL, (100mcg/mL) in 0.9% sodium chloride, Syringe, Rx Only, CAPS, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043
  • NDC72196-6009-1
Lot codes and dates
  • Lot

    192 of 192 codes

    • 36-239063
    • 36-239064
    • 36-239065
    • 36-239066
    • 36-239067
    • 36-23906
    • 736-239068
    • 36-239069
    • 36-239204
    • Exp. 7/10/2023
    • 36-239196
    • 36-239197
    • 36-239198
    • 36-239199
    • 36-239200
    • 36-239201
    • 36-239202
    • 36-239203
    • 36-239205
    • 36-239206
    • Exp. 7/11/2023
    • 36-239483
    • 36-239487
    • 36-239488
    • 36-239489
    • 36-239490
    • 36-239639
    • 36-239640
    • 36-239641
    • Exp. 7/12/2023
    • 36-239788
    • 36-239789
    • 36-239790
    • 36-239793
    • 36-239797
    • 36-239798
    • Exp. 7/13/2023
    • 36-240139
    • 36-240140
    • 36-240141
    • 36-240142
    • 36-240143
    • Exp. 7/16/2023
    • 36-240319
    • 36-240320
    • 36-240321
    • 36-240322
    • 36-240812
    • Exp. 7/17/2023
    • 36-241074
    • 36-241075
    • 36-241076
    • 36-241077
    • Exp. 7/18/2023
    • 36-241136
    • Exp. 7/19/2023
    • 36-241357
    • 36-241358
    • 36-241359
    • 36-241372
Amount recalled
499,304 Syringes

This recall covers 95 products

The agency filed one notice per product. You are reading one of them; the other 94 are below.

82 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Lack of assurance of sterility. Validation data for decontamination cycles is lacking.

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 28, 2025 · Data as of Sep 19, 8:07 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.