Mckesson Medical-Surgical Inc. Corporate Office 2024-03-20 Health serious FDA
Health · FDA · Recall #FDA-D-0373-2024
Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL,… Recall
Issued March 20, 2024 · Mckesson Medical-Surgical Inc. Corporate Office
In March 2024, Mckesson Medical-Surgical Inc. Corporate Office recalled the Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 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
cGMP Deviations: Products were stored outside the drug label specifications.
What you should do
- 1 Stop using Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Mckesson Medical-Surgical Inc. Corporate Office 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
- Mckesson Medical-Surgical Inc. Corporate Office
- Category
- Health
- Recall date
- March 20, 2024
- Units affected
- Not reported
- Sold at
- Product was distributed to three direct accounts in NM, AZ and UT.
- Recall number
- FDA-D-0373-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Mckesson Medical-Surgical Inc. Corporate Office has 76 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.