Baxter recalls Infuvite Adult multiple vitamins injections that may have been improperly stored during transit due to thunderstorms, risking product safety and effectiveness.
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.
Baxter is recalling Infuvite Adult multiple vitamins injections that were shipped in late March 2025 and delivered in early April 2025. These products may not have been stored at the correct temperature, which could affect their safety and effectiveness.
Severe thunderstorms caused delays in shipping these products, leading to improper storage conditions. This could affect the product's safety, quality, identity, potency, and purity.
People who received Infuvite Adult injections from this recall batch, typically those with prescriptions from healthcare providers. Patients using these injections for vitamin supplementation are most at risk.
Check for the product name 'Infuvite Adult', vials labeled 'Five of Vial 1 (5 mL)' and 'Five of Vial 2 (5 mL)', and the lot numbers AA2279 (expiring 8/31/26) or AA2383 (expiring 9/30/26).
Look for the lot numbers AA2279 or AA2383 on the vials to confirm if your product is affected.
Severe thunderstorms caused shipping delays, leading to improper storage conditions that may have affected the product's safety and effectiveness.
The recall does not specify a remedy, so check the product details to see if it's affected and contact your healthcare provider for guidance.
The recall indicates potential risks to safety and effectiveness, but no specific remedy is provided, so consult your healthcare provider.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall D-0401-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall D-0401-2025 from Baxter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
