Reported May 31, 2023 · Terminated

NORepinephrine added to 0.9% sodium chloride, 16 mg/250 mL* (64 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
    • 16 mg/250 mL* (64 mcg/mL)
    • 250 mL per bag
    • Rx only
    • Central Admixture Pharmacy Services
    • Inc
    • 6580 Snowdrift Rd
    • Ste 100
    • Allentown
    • PA 18106
    • NDC 71285-7036-1
Lot codes and dates
  • 88 of 88 codes

    • Lot # 37-882998
    • 37-883005
    • 37-883145
    • Exp 04/28/2023
    • 37-883144
    • 37-883220
    • 37-883221
    • 37-883222
    • Exp 04/30/2023
    • 37-883925
    • Exp 05/02/2023
    • 37-884180
    • 37-884181
    • Exp 05/03/2023
    • 37-884505
    • 37-884506
    • 37-884507
    • 37-884508
    • 37-884509
    • Exp 05/04/2023
    • 37-884834
    • 37-884869
    • 37-884870
    • Exp 05/07/2023
    • 37-886058
    • Exp 05/10/2023
    • 37-886536
    • 37-886537
    • Exp 05/14/2023
    • 37-887062
    • 37-887389
    • Exp 05/15/2023
    • 37-887784
    • 37-887787
    • Exp 05/17/2023
    • 37-888029
    • 37-888048
    • Exp 05/18/2023
    • 37-888261
    • 37-888263
    • 37-888269
    • 37-888282
    • 37-888292
    • 37-888294
    • 37-888301
    • 37-888302
    • Exp 05/21/2023
    • 37-890058
    • 37-890064
    • 37-890074
    • 37-890076
    • Exp 05/28/2023
    • 37-891747
    • 37-891748
    • 37-891750
    • 37-891751
    • 37-891753
    • Exp 06/04/2023
    • 37-893530
    • 37-893531
Amount recalled
6341 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, 5:04 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.