Bard Medical Division recalls SureStep Foley Tray Systems with specific product codes due to potential urine leakage around the vented sample port. Affected units include various model numbers and lot numbers listed in the recall notice.
potential for urine leakage around the vent on the vented sample port
Bard Medical Division is recalling SureStep Foley Tray Systems with specific product codes because they may leak urine around the vented sample port. This could lead to discomfort or infection for users.
The product may leak urine around the vented sample port due to a design issue, which could cause discomfort or increase the risk of infection for users. This is a minor hazard that does not pose a serious injury risk.
Healthcare professionals and patients using the SureStep Foley Tray System with the listed product codes and lot numbers are most at risk. The recall affects medical devices used for urinary catheter management.
Check the product code on the SureStep Foley Tray System (e.g., A119214M, A119216M, A119218M) and lot numbers listed in the recall notice. The product is used with catheters for urinary management.
Look for the product code on the SureStep Foley Tray System (e.g., A119214M, A119216M, A119218M) and lot numbers listed in the recall notice.
The product may leak urine around the vented sample port, which could cause discomfort or increase the risk of infection.
Check the product code and lot numbers listed in the recall notice. Affected units include specific model numbers and lot numbers provided in the record.
The recall does not specify a remedy, so contact Bard Medical Division directly 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-0803-2019 — Bard Medical Division Bard Medical Division Hello, I own a Bard Medical Division that is covered by recall Z-0803-2019 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.
