Fresenius Kabi recalls Sensorcaine injections with low epinephrine levels that may not work as intended. Affected batches expire 03/2024 or 05/2024. Stop using if you have these vials.
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Fresenius Kabi is recalling Sensorcaine injections due to testing showing the epinephrine content is below the required level. This could mean the product doesn't work properly during medical procedures, potentially leading to complications.
The product contains less epinephrine than it should, which may reduce its effectiveness during medical procedures. This could lead to inadequate pain control or unintended effects if used improperly.
Healthcare professionals who use Sensorcaine for procedures like nerve blocks. Patients receiving this injection are not directly affected since it's prescription-only.
Check for vials labeled 'Sensorcaine (Bupivacaine HCl and Epinephrine Injection, USP) with Epinephrine 1:200,000 (as bitartrate), 0.25%, 125 mg per 50 mL'. The batch numbers are 6128061 (exp 03/2024) or 6128663/6128664 (exp 05/2024).
Look for the product name and batch numbers listed in the recall notice to confirm if your vial is affected.
The recall states the epinephrine content is below the required level, which may reduce effectiveness but does not indicate immediate danger. Use only if the product is confirmed not recalled.
Check the vial label for the specific batch numbers: 6128061 (exp 03/2024) or 6128663/6128664 (exp 05/2024).
The recall does not specify a remedy, so contact Fresenius Kabi directly for guidance on disposal or alternatives.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0127-2023 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0127-2023 from Fresenius Kabi. 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.
