Bard recalls Optima Size 6 Fr. x 14 cm ureteral stent kits with possible label size discrepancies. Affected kits may not match actual product size, requiring verification before use.
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
Bard is recalling ureteral stent kits that might have incorrect size labels. This could lead to improper use if the stent doesn't match the label, potentially causing complications during medical procedures.
The stent's actual size might differ from what's labeled on the product. This discrepancy could lead to improper placement during medical procedures, potentially causing complications like blockages or infections.
Patients undergoing urological procedures who use Bard's Optima ureteral stent kits with the specific reference number 787614 are likely affected. Medical professionals and patients using these kits for procedures are at risk if the label size doesn't match the actual stent.
Check for the reference number 787614 on the kit packaging. The lot number NGJU4163/UDI: (01)00801741015403 is also associated with this recall. This kit was sold for medical use.
Check the product label against the actual stent size to ensure it matches the reference number 787614.
The recall addresses a labeling discrepancy that could lead to improper use, but it does not indicate a risk of serious injury or death. The danger level is low risk.
Look for the reference number 787614 and lot number NGJU4163/UDI: (01)00801741015403 on the kit packaging.
Verify the product label against the actual stent size to ensure it matches the reference number 787614. No immediate action is required beyond this check.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-0905-2026 — Bard Bard Hello, I own a Bard that is covered by recall Z-0905-2026 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.
