Central Admixture Pharmacy Services recalls Cardioplegia Solution (del Nido Formula) due to potential lack of sterility. Products with specific lot numbers and expiration dates are affected. This sterile solution is used in medical procedures and must be handled carefully.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services is recalling Cardioplegia Solution (del Nido Formula) because an FDA inspection found possible contamination. This sterile solution is used in medical procedures and must be discarded if you have the recalled lots.
The FDA inspection raised concerns that the solution might not be sterile. Since this product is used in critical medical procedures like heart surgery, contamination could lead to infections or other complications.
Healthcare professionals and medical facilities that use this sterile solution for cardiac surgery. Patients receiving the solution during procedures are at risk if the product was contaminated.
Check the product label for lot numbers: 37-890033, 37-890035, 37-890518, 37-890527, 37-890536, 37-890538, 37-890844, 37-890845, 37-891159, 37-891161, 37-891187, 37-891190, 37-891212, 37-891213, 37-891222, 37-891223, 37-891432, 37-891433, 37-891434, 37-891435, 37-891440, 37-891442, 37-891445, 37-891446, 37-891447, 37-891746, 37-891754, 37-891755, 37-892005, 37-892007, 37-892502, 37-892503, 37-892505, 37-892517, 37-892518, 37-892519, 37-892538, 37-892871, 37-892873, 37-892874, 37-892879, 37-892880, 37-892886, 37-892887, 37-892888, 37-892899, 37-893129, 37-893131, 37-893158, 37-893160, 37-893162, 37-893163, 37-893164, 37-893681, 37-893689, 37-893698, 37-893760, 37-893761, 37-893762, 37-894275, 37-894276, 37-894277, 37-894301, 37-894651, 37-894654, 37-894658, 37-894660, 37-894662, 37-894663, 37-894948, 37-894967, 37-894970, 37-895276, 37-895278, 37-895281, 37-895284, 37-895285, 37-895286, 37-895289, 37-895297, 37-895650, 37-895652, 37-896051, 37-896052, 37-896054, 37-896055, 37-896057, 37-896058, 37-896455, 37-896418, 37-896419, 37-896420, 37-896438, 37-896453, 37-896454, 37-896855, 37-896814, 37-896816, 37-896818, 37-896823, 37-896824, 37-896841, 37-896843, 37-896942, 37-897417, 37-897429, 37-897856, 37-897857, 37-897858, 37-897880, 37-897881, 37-897882, 37-898264, 37-898180, 37-898222, 37-898225, 37-898226, 37-898227, 37-898228, 37-898487, 37-898488, 37-898490, 37-898781, 37-898782, 37-898784, 37-898787, 37-898788, 37-899102, 37-899103, 37-899104, 37-899105, 37-899590, 37-899598, 37-899599, 37-900116, 3700000900051, 37-900052, 37-900054, 37-900055, 37-900306, 37-900309, 37-900310, 37-900311, 37-900313, 37-900314, 37-900315, 37-900316. The product is packaged in 1,052.8 mL bags and is prescription-only.
Look for the lot numbers listed in the recall notice to determine if your product is affected.
The FDA inspection raised concerns about sterility, but the product is not yet confirmed unsafe. Healthcare facilities should follow the recall instructions.
The recall does not specify a remedy, so contact Central Admixture Pharmacy Services for guidance.
Check the product label for the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Central Admixture Pharmacy Services to request your refund or repair — edit it as you like.
Subject: Recall D-0668-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0668-2023 from Central Admixture Pharmacy Services. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
