Reported Aug 9, 2023 · Terminated

oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL, IV Bag, Rx only, This drug was repacked by CAPS, 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?

  • oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL, IV Bag, Rx only, This drug was repacked by CAPS, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043
  • NDC72196-6044-1
Lot codes and dates
  • Lot

    366 of 366 codes

    • 36-238820
    • 36-238821
    • 36-238822
    • 36-238824
    • 36-238825
    • Exp. 7/10/2023
    • 36-239686
    • 36-239687
    • 36-239688
    • 36-239689
    • 36-239690
    • 36-239691
    • 36-239692
    • 36-239693
    • 36-239696
    • 36-239697
    • 36-239699
    • 36-239700
    • Exp. 7/12/2023
    • 36-239915
    • 36-239916
    • 36-239917
    • 36-239918
    • 36-239919
    • 36-239922
    • 36-239923
    • Exp. 7/13/2023
    • 36-240165
    • 36-240168
    • 36-240170
    • 36-240171
    • 36-240173
    • 36-240174
    • Exp. 7/16/2023
    • 36-240260
    • 36-240261
    • 36-240262
    • Exp. 7/17/2023
    • 36-240823
    • 36-240824
    • 36-240826
    • 36-240827
    • 36-240828
    • 36-240829
    • 36-240830
    • 36-240831
    • 36-240832
    • 36-240833
    • 36-240834
    • Exp. 7/18/2023
    • 36-241141
    • 36-241142
    • 36-241143
    • 36-241144
    • 36-241145
    • 36-241146
    • 36-241439
    • Exp. 7/19/2023
    • 36-241511
    • 36-241515
Amount recalled
130,250 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, 6:38 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.