Reported Aug 9, 2023 · Terminated

heparin 4000 units/1000mL added to 0.9% sodium chloride, 4 units/mL, IV Bag, Rx only, Cental Admixture Pharmacy…

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?

  • heparin 4000 units/1000mL added to 0.9% sodium chloride, 4 units/mL, IV Bag, Rx only, Cental Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043
  • NDC72196-7022-1
Lot codes and dates
  • Lot
    • 36-243555
    • 36-243556
    • Exp. 7/10/2023
    • 36-245117
    • 36-245118
    • 36-245119
    • 36-245120
    • Exp. 7/12/2023
    • 36-246163
    • 36-246164
    • Exp. 7/14/2023
    • 36-247010
    • Exp. 7/18/2023
    • 36-248226
    • 36-248229
    • 36-248232
    • 36-248248
    • Exp. 7/24/2023
    • 36-249829
    • 36-249830
    • 36-249831
    • 36-249832
    • Exp. 8/1/2023
    • 36-250047
    • 36-250048
    • 36-250049
    • 36-250050
    • Exp. 8/2/2023
    • 36-250289
    • 36-250290
    • 36-250291
    • 36-250293
    • Exp. 8/3/2023
    • 36-251057
    • 36-251058
    • 36-251060
    • Exp. 8/4/2023
    • 36-251385
    • 36-251386
    • 36-251387
    • 36-251388
    • Exp. 8/7/2023
    • 36-251448
    • 36-251449
    • 36-251450
    • Exp. 8/8/2023
    • 36-252462
    • Exp. 8/14/2023
    • 36-254679
    • 36-254681
    • Exp. 8/16/2023
    • 36-255116
    • 36-255117
    • 36-255118
    • Exp. 8/17/2023
    • 36-255488
    • Exp. 8/18/2023
Amount recalled
11,824 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, 8:09 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.