Reported May 31, 2023 · Terminated

NORepinephrine added to 0.9% sodium chloride, 8 mg/250 mL* (32 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?

    • NORepinephrine added to 0.9% sodium chloride
    • 8 mg/250 mL* (32 mcg/mL)
    • 250 mL per bag
    • Rx only
    • Central Admixture Pharmacy Services
    • Inc
    • 6580 Snowdrift Rd
    • Ste 100
    • Allentown
    • PA 18106
    • NDC 71285-8096-1
Lot codes and dates
    • Lot # 37-882989
    • Exp 04/28/2023
    • 37-883827
    • 37-883829
    • 37-883830
    • 37-883833
    • 37-883858
    • Exp 05/02/2023
    • 37-884758
    • Exp 05/05/2023
    • 37-885357
    • Exp 05/08/2023
    • 37-885748
    • 37-885751
    • Exp 05/09/2023
    • 37-887409
    • 37-887410
    • Exp 05/16/2023
    • 37-888863
    • 37-888867
    • Exp 05/22/2023
    • 37-889226
    • Exp 05/23/2023
    • 37-889576
    • 37-889577
    • Exp 05/24/2023
    • 37-889804
    • 37-889817
    • 37-889830
    • Exp 05/25/2023
    • 37-891280
    • Exp 05/31/2023
    • 37-891758
    • 37-891759
    • Exp 06/04/2023
    • 37-894311
    • 37-894315
    • 37-894319
    • Exp 06/13/2023
    • 37-895304
    • Exp 06/18/2023
    • 37-896544
    • 37-896545
    • 37-896546
    • 37-896552
    • Exp 06/21/2023
    • 37-898514
    • 37-898515
    • 37-898516
    • Exp 06/29/2023
    • 37-899305
    • Exp 07/03/2023
    • 37-900362
    • Exp 07/06/2023
Amount recalled
6414 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, 7:58 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.