Reported Aug 9, 2023 · Terminated

Cardioplegia Solution del Nido Formula, IV Bag, Total Volume = 1,052.8 mL, FOR INTRACARDIAC PERFUSION USE ONLY,…

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?

    • Cardioplegia Solution del Nido Formula
    • IV Bag
    • Total Volume = 1
    • 052.8 mL
    • FOR INTRACARDIAC PERFUSION USE ONLY
    • PLASMA-LYTE A 1000 mL
    • Mannitol 20% 16.3 mL
    • Sodium Bicarbonate 8.4% 13 mL
    • Potassium Chloride 2 mEq/mL 13 mL
    • Magnesium Sulfate 4.06 mEq/mL 4 mL
    • Lidocaine 2% 6.5 mL
    • Approx. Osmolarity 386 mOsm/L
    • Rx Only
    • Central Admixture Pharmacy Services
    • Inc
    • 2200 South 43rd Avenue
    • Phoenix
    • AZ 85043
  • NDC72196-0202-1
Lot codes and dates
  • Lot

    117 of 117 codes

    • 36-252365
    • 36-252368
    • 36-252369
    • 36-253887
    • 36-253888
    • Exp. 8/1/2023
    • 36-254404
    • 36-254406
    • 36-254407
    • 36-254408
    • 36-254409
    • 36-254410
    • Exp. 8/5/2023
    • 36-255219
    • 36-255220
    • 36-255221
    • 36-255222
    • 36-255223
    • Exp. 8/7/2023
    • 36-255420
    • 36-255421
    • 36-255422
    • 36-255424
    • 36-255425
    • 36-255453
    • 36-255454
    • 36-255731
    • Exp. 8/8/2023
    • 36-247605
    • 36-247608
    • 36-247609
    • 36-247610
    • Exp. 7/10/2023
    • 36-255880
    • 36-255881
    • 36-255882
    • 36-255883
    • 36-255884
    • 36-255885
    • 36-255887
    • 36-256004
    • Exp. 8/11/2023
    • 36-247819
    • 36-247820
    • 36-247821
    • 36-247822
    • Exp. 7/11/2023
    • 36-256108
    • 36-256109
    • 36-256110
    • 36-256111
    • 36-256112
    • 36-256113
    • Exp. 8/12/2023
    • 36-248139
    • 36-248142
    • 36-248143
    • 36-248144
    • Exp. 7/12/2023
    • 36-256326
Amount recalled
10,480 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, 6:39 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.