Baxter Healthcare recalls specific vascular probe models due to inaccurate marketing brochure content that conflicts with product instructions. Affected units include various lengths and sizes with unique product codes.
Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products Instructions for Use (IFU) or Prescribing Information (PI).
Baxter Healthcare is recalling specific vascular probes because their marketing brochures contain inaccurate information that doesn't match the product's instructions or prescribing details. This could lead to confusion in medical use, though no injuries have been reported.
The marketing brochures distributed for these probes contain information that doesn't align with the actual product instructions or prescribing details. This mismatch could cause confusion during medical procedures, potentially affecting treatment decisions.
Healthcare professionals and medical facilities that use Baxter Vascular Probes with the listed product codes. Patients using these probes during cardiovascular procedures may be at risk if they follow outdated marketing information.
Check the product code on the probe (e.g., 7081015, 7081520, 7082025) or the unique identification number (UDI/DI) listed in the recall notice. The probes come in different lengths (8cm, 15cm, 45cm) and sizes (1-1.5mm to 2-2.5mm).
Look for the product code on the probe, such as 7081015, 7081520, or 7082025, which corresponds to specific lengths and sizes.
The marketing brochures distributed for these probes contain inaccurate content that doesn't align with the product's instructions or prescribing details.
The affected models include vascular probes with product codes such as 7081015 (8cm, 1-1.5mm), 7081520 (8cm, 1.5-2mm), and others listed in the recall notice.
No action is required for safety, but healthcare professionals should verify the product's instructions before use to avoid confusion.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0659-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0659-2024 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.
