Reported Aug 9, 2023 · Terminated

fentaNYL in 0.9% sodium chloride, 2500 mcg/250 mL, (10 mcg/mL), 250 mL bag, Rx only, Central 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 · 7935 Dunbrook Rd Ste C · San Diego, CA · 92126-6322

Is this the product you have?

  • fentaNYL in 0.9% sodium chloride, 2500 mcg/250 mL, (10 mcg/mL), 250 mL bag, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2071-5
Lot codes and dates
  • Lot

    103 of 103 codes

    • 17-270584
    • 17-270586
    • 17-270597
    • 17-270613
    • Exp. 7/17/2023
    • 17-270655
    • 17-270659
    • 17-270741
    • Exp. 7/18/2023
    • 17-270872
    • 17-270875
    • Exp. 7/20/2023
    • 17-271040
    • 17-271041
    • 17-271042
    • 17-271058
    • 17-271066
    • 17-271071
    • 17-271080
    • Exp. 7/24/2023
    • 17-271111
    • 17-271148
    • 17-271150
    • 17-271151
    • 17-271152
    • 17-271166
    • Exp. 7/25/2023
    • 17-271241
    • 17-271267
    • Exp. 7/26/2023
    • 17-271402
    • 17-271407
    • 17-271413
    • 17-271429
    • Exp. 7/30/2023
    • 17-271555
    • 17-271556
    • 17-271560
    • 17-271594
    • Exp. 8/1/2023
    • 17-271754
    • Exp. 8/3/2023
    • 17-271797
    • 17-271799
    • 17-271821
    • 17-271842
    • Exp. 8/6/2023
    • 17-271888
    • 17-271889
    • Exp. 8/7/2023
    • 17-271949
    • 17-271950
    • Exp. 8/8/2023
    • 17-272021
    • 17-272041
    • Exp. 8/9/2023
    • 17-272285
    • 17-272292
    • 17-272309
    • 17-272316
Amount recalled
8,146 bags

This recall covers 39 products

The agency filed one notice per product. You are reading one of them; the other 38 are below.

26 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Lack of assurance of sterility: Lack of validation data for sanitization cycles

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 21, 2025 · Data as of Sep 19, 8:38 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.