Reported Aug 9, 2023 · Terminated

EPINEPHrine 4mg/250mL added to 0.9% sodium chloride, IV Bag, RX only, Central Admixture Pharmacy Services, Inc., 2200…

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?

  • EPINEPHrine 4mg/250mL added to 0.9% sodium chloride, IV Bag, RX only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043
  • NDC72196-8093-1
Lot codes and dates
  • Lot
    • 36-239250
    • Exp. 7/10/2023
    • 36-240225
    • Exp.7/16/2023
    • 36-241268
    • 36-241270
    • Exp. 7/19/2023
    • 36-241443
    • Exp. 7/20/2023
    • 36-242436
    • 36-242439
    • Exp. 7/25/2023
    • 36-241443
    • Exp. 7/20/2023
    • 36-242436
    • 36-242439
    • Exp. 7/25/2023
    • 36-243517
    • 36-243738
    • Exp. 7/30/2023
    • 36-245656
    • Exp. 8/2/2023
    • 36-246154
    • 36-246169
    • 36-246672
    • 36-246673
    • 36-246674
    • Exp. 8/3/2023
    • 36-247015
    • 36-247016
    • 36-247017
    • Exp. 8/7/2023
    • 36-247339
    • 36-247341
    • 36-247342
    • 36-247343
    • Exp. 8/8/2023
    • 36-249466
    • 36-249467
    • Exp. 8/17/2023
    • 36-249591
    • 36-249592
    • Exp. 8/18/2023
    • 36-251338
    • Exp. 8/27/2023
    • 36-251940
    • Exp. 8/30/2023
    • 36-254371
    • 36-254372
    • 36-254373
    • 36-254375
    • Exp. 9/4/2023
Amount recalled
9,121 bags

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, 5:08 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.