Reported May 31, 2023 · Terminated

PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 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
    • 40 mg/250 mL* (160 mcg/mL)
    • 250 mL per bag
    • Rx only
    • Central Admixture Pharmacy Services
    • Inc
    • 6580 Snowdrift Rd
    • Ste 100
    • Allentown
    • PA 18106
    • NDC 71285-6092-1
Lot codes and dates
    • Lot # 37-883910
    • Exp 05/02/2023
    • 37-884221
    • Exp 05/03/2023
    • 37-884756
    • Exp 05/05/2023
    • 37-885358
    • Exp 05/08/2023
    • 37-885683
    • Exp 05/09/2023
    • 37-886267
    • 37-886268
    • Exp 05/11/2023
    • 37-886539
    • Exp 05/14/2023
    • 37-887458
    • 37-887459
    • Exp 05/16/2023
    • 37-888080
    • Exp 05/18/2023
    • 37-889192
    • Exp 05/23/2023
    • 37-889575
    • 37-889578
    • Exp 05/24/2023
    • 37-889852
    • 37-889855
    • Exp 05/25/2023
    • 37-890120
    • 37-890126
    • Exp 05/28/2023
    • 37-891485
    • 37-891491
    • Exp 06/01/2023
    • 37-892901
    • 37-892966
    • Exp 06/07/2023
    • 37-893236
    • 37-893237
    • Exp 06/08/2023
    • 37-893997
    • Exp 06/12/2023
    • 37-894777
    • Exp 06/14/2023
    • 37-895317
    • 37-895321
    • 37-895323
    • Exp 06/18/2023
    • 37-896201
    • Exp 06/20/2023
    • 37-896923
    • Exp 06/22/2023
    • 37-898558
    • Exp 06/29/2023
Amount recalled
14205 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, 5:55 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.