SCA Pharmaceuticals recalls fentanyl injections with potential lack of sterility. This could cause infections if used improperly. Check your product details and contact the company for action steps.
Lack of Assurance of Sterility
SCA Pharmaceuticals is recalling fentanyl injections that may not be sterile, which could lead to infections if used. This recall affects patients who have been prescribed these injections for epidural use.
The injections may not be sterile, which could lead to infections if used. This is a risk for patients receiving epidural anesthesia treatments.
Patients prescribed fentanyl injections for epidural use. Those with the specific product details listed in the recall are most at risk.
Check for the product name: fentanyl 100 mcg/50 mL with bupivacaine. Look for the lot number 1223049125 and expiration date 12/04/23 on the packaging.
Verify the lot number 1223049125 and expiration date 12/04/23 on the injection packaging.
The recall states there is a lack of assurance of sterility, which could lead to infections. Do not use the product until the manufacturer provides instructions.
The recall does not specify a remedy, so contact SCA Pharmaceuticals for guidance.
Look for the lot number 1223049125 and expiration date 12/04/23 on the injection packaging.
We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0399-2024 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0399-2024 from SCA Pharmaceuticals. 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.
