Baxter Healthcare recalls surgical tools brochures with inaccurate content that doesn't match product instructions. Affected items include Flo-Thru Intraluminal Shunts with specific serial numbers. Consumers should check if they have these brochures.
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 recall matters because incorrect information could lead to improper use of medical devices, potentially causing harm during procedures.
The brochures contain inaccurate content that does not align with the products' Instructions for Use. This mismatch could lead to improper use of medical devices during procedures, potentially causing harm to patients or the user.
Healthcare professionals who use Baxter's Flo-Thru Intraluminal Shunts may be affected. Those with the specific brochures or devices listed in the recall are most at risk.
Check for brochures with reference numbers US-AS18-210002, US-AS18-210004, or US-AS46-230002. Affected Flo-Thru Intraluminal Shunts have specific serial numbers listed in the recall.
Look for brochures with reference numbers US-AS18-210002, US-AS18-210004, or US-AS46-230002.
Check if your Flo-Thru Intraluminal Shunt has serial numbers matching the list provided in the recall.
The brochures contain inaccurate content that does not align with the products' Instructions for Use, which could lead to improper use during procedures.
Flo-Thru Intraluminal Shunts with specific serial numbers listed in the recall, including models FT12100 through FT12300.
No action is needed if you do not have the affected brochures or devices. The recall only applies to those with the specific items listed.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1523-2024 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-1523-2024 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.
