Reported May 31, 2023 · Terminated

oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc.,…

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?

  • oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6044-1.
Lot codes and dates
  • 320 of 320 codes

    • Lot # 37-883041
    • 37-883043
    • 37-883044
    • 37-883045
    • 37-883047
    • 37-883059
    • 37-883060
    • 37-883067
    • 37-883071
    • 37-883072
    • 37-883131
    • 37-883185
    • Exp 04/28/2023
    • 37-883492
    • 37-883499
    • 37-883501
    • 37-883503
    • 37-883514
    • 37-883525
    • 37-883526
    • 37-883539
    • 37-883540
    • 37-883548
    • 37-883549
    • 37-883550
    • 37-883551
    • Exp 05/01/2023
    • 37-884229
    • 37-884230
    • 37-884245
    • 37-884249
    • 37-884252
    • 37-884256
    • 37-884260
    • 37-884261
    • 37-884262
    • 37-884266
    • 37-884270
    • Exp 05/03/2023
    • 37-884452
    • 37-884453
    • 37-884457
    • 37-884461
    • 37-884464
    • 37-884466
    • 37-884468
    • 37-884470
    • 37-884472
    • 37-884473
    • Exp 05/04/2023
    • 37-884793
    • 37-884812
    • 37-884817
    • 37-884821
    • 37-884822
    • 37-884830
    • 37-884833
    • 37-884874
    • 37-884881
    • 37-884886
Amount recalled
104807 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, 7:22 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.