Central Admixture Pharmacy Services recalls HyperLyte CR Injection due to potential contamination in sterile products. Affected lots expire by May 2023. Consumers should not use these products.
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 HyperLyte CR Injection (250 mL bags) because an FDA inspection raised concerns about the sterility of the products. This could lead to infections if used improperly.
The products were found to lack sterility during an FDA inspection. If contaminated, they could cause serious infections in patients who receive them through intravenous administration.
Healthcare professionals and patients who have received the recalled HyperLyte CR Injection. Those using the product for medical treatments are at risk of infection.
Check the lot numbers: 37-885553, 37-885554, 37-887923, 37-887924, 37-890778, 37-890779, 37-892847, 37-895049, 37-898480, 37-898481. Products expire by May 2023.
Immediately discard any HyperLyte CR Injection products with the affected lot numbers listed in the recall notice.
The products lack sterility as confirmed by an FDA inspection, which could lead to infections if used.
Check the lot numbers on the product: 37-885553, 37-885554, 37-887923, 37-887924, 37-890778, 37-890779, 37-892847, 37-895049, 37-898480, 37-898481. Products expire by May 2023.
The recall does not mention replacements or refunds; the remedy is to stop using and discard the product.
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-0755-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0755-2023 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.
