Baxter Healthcare recalls surgical tools and cardiovascular brochures with inaccurate content that doesn't match product instructions. Affected items include Flo-Rester and Vascular Probe models with specific serial numbers.
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 providers rely on the incorrect content.
The marketing brochures contain information that does not match the actual product instructions. This could cause healthcare providers to use the devices incorrectly, potentially leading to improper medical procedures or complications during treatment.
Healthcare providers who use Flo-Rester Disposable Internal Vessel Occluder or Vascular Probe Intravascular Probe devices with the listed serial numbers are most at risk. The recall affects medical professionals and facilities that use these specific products.
Check if you have the Flo-Rester Disposable Internal Vessel Occluder with serial numbers listed in the recall (e.g., 50100, 50125, etc.). Also, verify if you have the Cardiovascular Specialty marketing brochures with reference numbers US-AS18-210002, US-AS18-210004, or US-AS46-230002.
Look for the specific serial numbers listed in the recall for Flo-Rester devices (e.g., 50100, 50125, etc.) to determine if your item is affected.
Check if you have the Cardiovascular Specialty marketing brochures with reference numbers US-AS18-210002, US-AS18-210004, or US-AS46-230002 to see if they contain inaccurate content.
The recall affects Flo-Rester Disposable Internal Vessel Occluder with specific serial numbers (e.g., 50100, 50125) and Cardiovascular Specialty marketing brochures with reference numbers US-AS18-210002, US-AS18-210004, and US-AS46-230002.
The marketing brochures contain inaccurate content that does not align with the products' Instructions for Use, which could lead to improper use of medical devices.
The recall does not require immediate action, but you should check the serial numbers and marketing brochures to ensure you have the correct information for safe use.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1522-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1522-2024 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.
