Fresenius Kabi recalls Sensorcaine-MPF injections with low epinephrine levels. This may cause ineffective anesthesia during procedures. Contact for details.
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Fresenius Kabi is recalling Sensorcaine-MPF injections that have been tested with epinephrine levels below the required standard. Using these injections could lead to ineffective anesthesia during medical procedures.
The epinephrine concentration in these injections is lower than required. This could result in the injection being less effective for numbing pain during medical procedures.
Healthcare professionals who use Sensorcaine-MPF for anesthesia procedures. Patients receiving this injection may not get proper pain relief.
Check for the product name Sensorcaine-MPF with Epinephrine 1:200,000 (as bitartrate), 0.25%, 25 mg per 10 mL. Look for the NDC 63323-468-01 vial and NDC 63323-468-17 tray packaging. The batch number 6128800 with expiration 12/2023.
Identify the product by checking the NDC 63323-468-01 vial and NDC 63323-468-17 tray packaging.
The product has been tested with epinephrine levels below the defined limit, which could lead to ineffective anesthesia.
The recall record does not specify a remedy, so contact Fresenius Kabi for further instructions.
The product may not be effective due to low epinephrine levels, but the recall record does not indicate immediate danger.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0129-2023 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0129-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.