C.R. Bard recalls BD InLay Optima Ureteral Stent Kit (4.7 Fr. x 26 cm, REF 788426) due to potential size mismatch with product label. Affected units may have incorrect dimensions.
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
C.R. Bard is recalling a specific ureteral stent kit because the actual size might not match what's on the label. This could lead to improper use if the stent is too large or too small for the patient's ureter.
The stent's actual size might differ from what's listed on the product label. This could mean the stent is too large or too small for the patient's ureter, potentially causing complications during medical procedures.
Patients who have received this specific ureteral stent kit for medical procedures are likely affected. Medical professionals using the kit during procedures may also be at risk if the size discrepancy causes improper placement.
Check for the product name 'BD InLay Optima Ureteral Stent Kit', size 4.7 Fr. x 26 cm, and reference number REF 788426. Lot numbers NGJU4181 or UDI: (01)00801741015687 may also be present.
Verify the stent size matches the label; if it does not, contact your healthcare provider.
The recall is due to a labeling discrepancy, not a safety issue with proper use. The risk is low if the stent size matches the label.
Check the label against the product specifications; if there's a mismatch, contact your healthcare provider.
Look for the product name 'BD InLay Optima Ureteral Stent Kit', size 4.7 Fr. x 26 cm, and reference number REF 788426.
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-0906-2026 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-0906-2026 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.
