Reported May 31, 2023 · Terminated

PHENYLephrine added to 0.9% sodium chloride, 20 mg/250 mL* (80 mcg/mL), 250 mL per bag, 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. · 6580 Snowdrift Rd Ste 100 · Allentown, PA · 18106-9331

Is this the product you have?

    • PHENYLephrine added to 0.9% sodium chloride
    • 20 mg/250 mL* (80 mcg/mL)
    • 250 mL per bag
    • Rx only
    • Central Admixture Pharmacy Services
    • Inc
    • 6580 Snowdrift Rd
    • Ste 100
    • Allentown
    • PA 18106
    • NDC 71285-7025-1
Lot codes and dates
    • Lot # 37-883074
    • Exp 04/28/2023
    • 37-883237
    • 37-883238
    • Exp 04/30/2023
    • 37-883940
    • Exp 05/02/2023
    • 37-884271
    • Exp 05/03/2023
    • 37-884749
    • 37-884751
    • Exp 05/05/2023
    • 37-885338
    • Exp 05/08/2023
    • 37-885756
    • Exp 05/09/2023
    • 37-886272
    • Exp 05/11/2023
    • 37-887512
    • Exp 05/16/2023
    • 37-888027
    • 37-888030
    • 37-888040
    • 37-888052
    • 37-888063
    • Exp 05/18/2023
    • 37-888314
    • Exp 05/21/2023
    • 37-890489
    • 37-890497
    • 37-890534
    • Exp 05/29/2023
    • 37-890933
    • Exp 05/30/2023
    • 37-891152
    • Exp 05/31/2023
    • 37-892985
    • 37-892986
    • 37-892995
    • Exp 06/07/2023
    • 37-893511
    • 37-893517
    • Exp 06/11/2023
    • 37-896481
    • Exp 06/21/2023
    • 37-897828
    • Exp 06/27/2023
    • 37-898523
    • Exp 06/29/2023
Amount recalled
13953 bags

This recall covers 108 products

The agency filed one notice per product. You are reading one of them; the other 107 are below.

95 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

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 Jun 22, 2025 · Data as of Sep 19, 6:36 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.