Reported Aug 9, 2023 · Terminated

succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, 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?

  • succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue Pheonix, AZ, NDC 72196-6011-2.
Lot codes and dates
  • Lot

    99 of 99 codes

    • 36-238812
    • 36-238813
    • 36-238814
    • 36-238815
    • 36-238816
    • 36-238819
    • Exp. 7/10/2023
    • 36-239281
    • 36-239282
    • 36-239284
    • Exp. 7/11/2023
    • 36-239459
    • 36-239460
    • 36-239628
    • 36-239629
    • Exp. 7/12/2023
    • 36-239879
    • 36-239880
    • 36-239881
    • Exp. 7/13/2023
    • 36-240272
    • Exp. 7/16/2023
    • 36-240512
    • 36-240513
    • 36-240514
    • 36-240515
    • 36-240724
    • Exp. 7/17/2023
    • 36-240991
    • 36-240992
    • 36-240993
    • Exp. 7/18/2023
    • 36-241267
    • 36-241269
    • Exp. 7/19/2023
    • 36-241364
    • 36-241366
    • 36-241367
    • 36-241368
    • Exp. 7/20/2023
    • 36-241669
    • 36-241670
    • 36-241735
    • Exp. 7/21/2023
    • 36-242079
    • 36-242080
    • 36-242081
    • 36-242082
    • 36-242083
    • 36-242084
    • 36-242085
    • Exp. 7/24/2023
    • 36-242624
    • 36-242627
    • 36-242628
    • 36-242629
    • Exp. 7/26/2023
    • 36-243046
    • 36-243047
    • 36-243048
Amount recalled
26,208 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, 7:24 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.