Baxter Healthcare recalls Vascu-Guard Peripheral Vascular Patches due to inaccurate marketing brochure content conflicting with product instructions. Affected product codes include VG0108, VG0110, VG0106, and VG0209.
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 certain Vascu-Guard Peripheral Vascular Patches because marketing brochures contain inaccurate information that doesn't match the product's instructions or prescribing details. This could lead to confusion about how to use the patches safely.
The marketing brochure contains information that doesn't align with the product's actual instructions or prescribing details. This mismatch could cause confusion about proper use, but it does not pose a direct safety risk during normal use.
Healthcare professionals and patients using Baxter's Vascu-Guard patches for cardiovascular surgery may be affected. Those with the specific product codes listed are most at risk.
Check for product codes: VG0108 (0.8 x 8 cm), VG0110 (1 x 10 cm), VG0106 (1 x 6 cm), or VG0209 (2 x 9 cm). The patches also have specific UDI/DI numbers: 0338-9564-06 to 0338-9564-09.
Look for the product codes listed: VG0108, VG0110, VG0106, or VG0209.
The marketing brochure contains inaccurate content that doesn't align with the product's instructions or prescribing details.
Product codes: VG0108 (0.8 x 8 cm), VG0110 (1 x 10 cm), VG0106 (1 x 6 cm), and VG0209 (2 x 9 cm).
No, the recall is for inaccurate marketing information, not a safety hazard. You can continue using the patches as normal.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0666-2024 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-0666-2024 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.
