PFIZER 2024-01-31 Health critical FDA
Health · FDA · Recall #FDA-D-0261-2024
Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx… Recall
Issued January 31, 2024 · PFIZER
In January 2024, PFIZER recalled the Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx…, a critical 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
Presence of particulate matter: glass
What you should do
- 1 Stop using Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact PFIZER to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- PFIZER
- Category
- Health
- Recall date
- January 31, 2024
- Units affected
- Not reported
- Sold at
- Nationwide in the USA, Netherlands and Libya
- Recall number
- FDA-D-0261-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- PFIZER has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.