Bard recalls specific Broviac and Hickman catheter cutdown trays with SureCuff cuffs due to potential damage to the outer tray that could compromise the sterile barrier. Affected products include various sizes and models with catalog numbers 600060-606560.
Due to damage to outer tray that can potentially compromise the sterile barrier
Bard is recalling several types of catheter cutdown trays with SureCuff cuffs because the outer tray may have damage that could compromise the sterile barrier. This could lead to infection or other complications during medical procedures.
The outer tray of the device may have damage that could compromise the sterile barrier, potentially leading to infection or contamination during medical procedures. This is a risk during the insertion or use of the catheter.
Healthcare professionals using these specific catheter cutdown trays for medical procedures are most at risk. Patients using these devices under medical supervision are not directly affected.
Check for products with catalog numbers 600060 to 606560, including specific lot numbers listed in the recall notice. The product names include Broviac and Hickman catheter cutdown trays with SureCuff cuffs.
Review the product catalog number and lot number to confirm if your device is affected.
No, the recall does not require immediate discontinuation. The hazard is low risk and does not pose a serious injury risk in normal use.
Check the product catalog number and lot number listed in the recall notice. Affected products have catalog numbers from 600060 to 606560 with specific lot numbers.
Contact Bard directly to confirm if your product is affected and follow their instructions for replacement or return.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1367-2026 — Bard Bard Hello, I own a Bard that is covered by recall Z-1367-2026 from Bard. 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.
