C.R. Bard recalls female intermittent urinary catheters with specific catalog numbers and lot numbers due to a packaging defect that may compromise sterility. Affected units include REF 51808-51818 models.
Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.
C.R. Bard is recalling certain female intermittent urinary catheters because a manufacturing defect in the packaging could allow contamination, risking infection. This affects specific catalog numbers and lot numbers listed in the recall.
The catheters had a defect where the clear resealing label could separate from the foil pouch, potentially creating an opening that might allow contaminants to enter the sterile packaging. This could lead to infection if the catheter is used without proper sterility.
Women using the recalled catheters for urinary drainage are most at risk. The recall targets specific model numbers and production lots.
Check for catalog numbers REF 51808, REF 51810, REF 51812, REF 51814, REF 51816, or REF 51818. Also look for specific lot numbers listed in the recall notice.
Review the catalog number and lot number on the catheter packaging to determine if it is affected by this recall.
The recall is due to a manufacturing defect where the clear resealing label could separate from the foil pouch, potentially allowing contaminants to enter the sterile packaging.
Check the catalog number and lot number on the catheter packaging. If it matches the recalled items, contact C.R. Bard for instructions.
The defect could compromise sterility, increasing the risk of infection if the catheter is used without proper sterile conditions.
We’ve drafted a message you can send C.R. Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1698-2023 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-1698-2023 from C.R. 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.
