Baxter recalls specific acetaminophen injection vials due to temperature storage risk. Product labeled for room temperature but shipped refrigerated, potentially causing instability.
Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product is labeled to be stored in a controlled room temperature environment.
Baxter is recalling certain acetaminophen injections because they were shipped in refrigerated trucks but labeled for room temperature storage. This could lead to product instability if stored incorrectly.
The product was distributed in refrigerated trucks with labels indicating 'Refrigerate Upon Arrival', but the product is labeled for room temperature storage. This mismatch could cause the product to become unstable if stored in a refrigerated environment.
Healthcare professionals using the recalled acetaminophen injections for intravenous administration. Patients receiving these injections are at risk if the product was improperly stored.
Check for the product name 'Acetaminophen Injection, 10 mg/mL, 1,000 mg/100 mL, 100 mL VIAFLO container bag, Single Dose Container'. Look for lot numbers: 20K19G64T1 (exp 10/31/2022), 21K23G65 (exp 10/31/2023), or 21L10G65 (exp 11/30/2023).
Look for the lot numbers listed in the recall notice: 20K19G64T1 (exp 10/31/2022), 21K23G65 (exp 10/31/2023), or 21L10G65 (exp 11/30/2023).
The product is safe if stored at room temperature as labeled. However, if it was stored in refrigeration, it may become unstable.
Check the product label for the lot numbers: 20K19G64T1 (exp 10/31/2022), 21K23G65 (exp 10/31/2023), or 21L10G65 (exp 11/30/2023).
The recall does not specify a remedy, so contact Baxter Healthcare Corporation for guidance on safe handling or disposal.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall D-1348-2022 — Baxter Baxter Hello, I own a Baxter that is covered by recall D-1348-2022 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.
