The Recall Desk
HighFDA (Drugs)·D-0401-2025·Announced 2025-05-07

[pending] INFUVITE ADULT (MULTIPLE VITAMINS INJECTION)

Pending LLM rewrite. Source: FDA_DRUG D-0401-2025.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Pending LLM scoring against the rubric.

Plain-English summary

Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.

The recalled product

Product
INFUVITE ADULT (MULTIPLE VITAMINS INJECTION)
Brand
INFUVITE ADULT
Manufacturer
Mckesson Medical-Surgical Inc. Corporate Office

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

  • Lot #: AA2279
  • Exp 8/31/26
  • AA2383
  • Exp 9/30/26

Distribution

Distributed in 2 states:

  • FL
  • MS