Baxter Healthcare recalls surgical tools and cardiovascular brochures with inaccurate content that doesn't match product instructions. Affected items include specific vascular probes and shunts. Consumers should check product details to determine if they are affected.
The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products Instructions for Use (IFU).
Baxter Healthcare is recalling surgical tools and cardiovascular specialty marketing brochures that contain inaccurate information compared to the product's instructions for use. This could lead to improper use of medical devices if healthcare professionals rely on the incorrect content.
The brochures contain information that does not align with the actual product instructions for use. This could result in incorrect application of medical devices if healthcare workers rely on the inaccurate content. However, the hazard is not a physical risk like injury or fire but rather a potential for misuse due to misleading information.
Healthcare professionals who use Baxter's surgical tools and cardiovascular specialty brochures may be affected. Those most at risk are medical staff handling the specific vascular probes and shunts listed in the recall.
Check for the reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, or US-AS46-230002 CV Specialty Brochure US version. Affected items include specific vascular probes with item numbers like 7081015 and shunts with serial numbers starting with 7081015.
Review the product's reference numbers and item numbers to determine if it matches the recalled items listed in the notice.
The recall affects specific vascular probes with item numbers like 7081015 and shunts with serial numbers starting with 7081015, as well as the mentioned brochures and website versions.
The brochures contain inaccurate content that does not align with the products' Instructions for Use, which could lead to improper use if healthcare professionals rely on the incorrect information.
No action is required to stop using the products, but you should check if your items match the recalled list to ensure you have accurate information.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1524-2024 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-1524-2024 from Baxter Healthcare. 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.
