Reported Aug 9, 2023 · Terminated

rocuronium50 mg/5 mL (10 mg/mL), Syringes Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue,…

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?

  • rocuronium50 mg/5 mL (10 mg/mL), Syringes Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue, Pheonix, AZ, NDC 72196-6010-1.
Lot codes and dates
  • Lot

    113 of 113 codes

    • 36-238805
    • 36-238806
    • 36-238808
    • 36-238809
    • 36-238810
    • 36-238811
    • Exp. 7/10/2023
    • 36-239229
    • 36-239319
    • 36-239320
    • 36-239321
    • 36-239322
    • Exp. 7/11/2023
    • 36-239453
    • 36-239454
    • 36-239455
    • Exp. 7/12/2023
    • 36-239851
    • 36-239852
    • Exp. 7/13/2023
    • 36-240204
    • Exp. 7/16/2023
    • 36-240509
    • 36-240510
    • 36-240511
    • Exp. 7/17/2023
    • 36-241263
    • 36-241266
    • Exp. 7/19/2023
    • 36-241362
    • 36-241363
    • 36-241365
    • Exp. 7/20/2023
    • 36-241880
    • 36-241881
    • 36-241882
    • Exp. 7/23/2023
    • 36-242376
    • 36-242377
    • Exp. 7/24/2023
    • 36-242603
    • 36-242618
    • Exp. 7/25/2023
    • 36-242643
    • 36-242644
    • 36-242645
    • Exp. 7/26/2023
    • 36-243534
    • 36-243535
    • Exp. 7/30/2023
    • 36-243831
    • Exp. 7/31/2023
    • 36-244831
    • 36-244833
    • 36-244841
    • 36-244842
    • 36-244845
    • 36-244855
    • Exp. 8/01/2023
    • 36-245803
Amount recalled
77,554 Syringes.

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, 5:56 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.