C.R. Bard recalls pediatric Magic3 Go intermittent urinary catheters with a possible sterility risk due to a packaging defect that could allow product opening.
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 pediatric Magic3 Go intermittent urinary catheters with catalog number REF 52810G. The recall is due to a manufacturing defect that could compromise product sterility if the resealing label separates from the foil pouch.
The defect involves the resealing label separating from the foil pouch, which could create an opening in the packaging. This might allow contamination and impact product sterility, potentially leading to infection risks.
Pediatric patients using Magic3 Go intermittent urinary catheters with catalog number REF 52810G are affected. Parents and caregivers of children with urinary catheters are most at risk.
Check for the catalog number REF 52810G on the catheter packaging. The lot number JUGW1445 is also associated with this recall.
Look for the catalog number REF 52810G and lot number JUGW1445 on the catheter packaging.
The recall is due to a manufacturing defect where the resealing label could separate from the foil pouch, potentially compromising product sterility.
Check for the catalog number REF 52810G and lot number JUGW1445 on the packaging.
The recall record does not specify a remedy, so contact C.R. Bard for further instructions.
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-1700-2023 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-1700-2023 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.
