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Mckesson Medical-Surgical Inc. Corporate Office — Infuvite Adult Multiple vitamins injection, single-dose vial 5mL, Rx only, MFG: Baxter Healthcare Corp., NDC 54643-5649-01
Check whether yours is affected, then follow the instructions below.
What’s wrong
cGMP Deviations: Products were stored outside the drug label specifications.
The Recall Registry rates this serious — FDA Class II: temporary or medically reversible health harm.
What to do
Check the lot numbers below against what you have, and follow the FDA recall notice for what to do with the affected product. If you use it daily, or it is for a child, your pharmacist can tell you whether it matters and what to use instead.
Who to contact: Recalling firm: Mckesson Medical-Surgical Inc. Corporate Office
The product
Infuvite Adult Multiple vitamins injection, single-dose vial 5mL, Rx only, MFG: Baxter Healthcare Corp., NDC 54643-5649-01
Details
- Units affected
- 70 vials
- Recall date
- February 7, 2024
- Brand
- Mckesson Medical-Surgical Inc. Corporate Office
Product was distributed to three direct accounts in NM, AZ and UT
The official notice
This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.
Their exact wording: “Mckesson Medical-Surgical Inc. Corporate Office — Infuvite Adult Multiple vitamins injection, single-dose vial 5mL, Rx only, MFG: Baxter Healthcare Corp., NDC 54643-5649-01”
Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.
Filed under: Over-the-counter & supplements