Bard Medical Division recalls SureStep Foley Tray Systems with catalog number A319418AM and lot NGCT1929 due to potential urine leaks from vented sample ports. Affected units may require replacement to prevent infection.
Some SureStep" Foley Tray Systems with product catalog number A319418AM and lot number NGCT1929 contain vented sample ports that may have an increased likelihood of leaking urine from the vent on the sample port.
Bard Medical Division is recalling SureStep Foley Tray Systems with specific catalog and lot numbers because they may leak urine from sample ports. This could lead to infection risks if urine leaks into the system.
The vented sample ports in some units may leak urine, which could introduce bacteria into the system. This increases the risk of urinary tract infections if urine leaks into the catheter or surrounding areas.
Patients using the SureStep Foley Tray System with catalog number A319418AM and lot number NGCT1929 are affected. Healthcare providers and caregivers who use these systems are most at risk of infection.
Check for product catalog number A319418AM and lot number NGCT1929 on the SureStep Foley Tray System. These units were sold with an expiration date of November 30, 2018.
Verify the catalog number (A319418AM) and lot number (NGCT1929) on your SureStep Foley Tray System.
The recall is due to potential urine leaks from vented sample ports in some units, which could increase infection risk.
Check for product catalog number A319418AM and lot number NGCT1929 on the SureStep Foley Tray System.
The recall does not specify a remedy, so contact Bard Medical Division for further instructions.
We’ve drafted a message you can send Bard Medical Division to request your refund or repair — edit it as you like.
Subject: Recall Z-0800-2019 — Bard Medical Division Bard Medical Division Hello, I own a Bard Medical Division that is covered by recall Z-0800-2019 from Bard Medical Division. 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.
