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Serious recall: Injury is possible or has been reported. Take action promptly.

SCA Pharmaceuticals, LLC 2024-04-03 Health serious FDA
Health · FDA · Recall #FDA-D-0403-2024

fentaNYL 2,500 mcg/50 mL in 0.9 % Sodium Chloride Injection (Concentration = 50 mcg/mL)… Recall

Issued April 3, 2024 · SCA Pharmaceuticals, LLC

In April 2024, SCA Pharmaceuticals, LLC recalled the fentaNYL 2,500 mcg/50 mL in 0.9 % Sodium Chloride Injection (Concentration = 50 mcg/mL)…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Lack of Assurance of Sterility

What you should do

  1. 1 Stop using fentaNYL 2,500 mcg/50 mL in 0.9 % Sodium Chloride Injection (Concentration = 50 mcg/mL)… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact SCA Pharmaceuticals, LLC to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
SCA Pharmaceuticals, LLC
Category
Health
Recall date
April 3, 2024
Units affected
Not reported
Sold at
Nationwide in the USA
Recall number
FDA-D-0403-2024
Made in
United States
Issuing agency
FDA

In context

  • SCA Pharmaceuticals, LLC has 15 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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