Bard recalls two types of 9.5mm dual-lumen catheters that may contain incorrect barb tips, potentially prolonging medical procedures. Affected units have specific reference and lot numbers.
Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
Bard is recalling two specific catheter models that might have the wrong barb tip design. This could lead to longer medical procedures than intended. The recall affects certain production batches with known reference and lot numbers.
The catheters might include a tunneler with a barb tip designed for a smaller catheter (6Fr) instead of the correct size (9.6Fr). This mismatch could cause the procedure to take longer than necessary, potentially increasing patient risk.
Healthcare professionals using the recalled catheters are most at risk. Patients receiving these catheters during procedures may be affected if the incorrect tip causes delays.
Check for the reference numbers 7726950 or 7726954 on the catheter packaging. The lot numbers RECQ1106 (for 7726950) and RECU1837 (for 7726954) are also listed in the recall.
Look for the reference numbers 7726950 or 7726954 and lot numbers RECQ1106 or RECU1837 on the catheter packaging.
The product may contain a tunneler with a barb tip meant for a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter, which could prolong medical procedures.
Check the reference and lot numbers on the packaging. If they match the recalled units, contact Bard for further instructions.
The recall states a potential for prolonged operations, but no specific injury mechanism is mentioned. The hazard level is low risk.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1574-2020 — Bard Bard Hello, I own a Bard that is covered by recall Z-1574-2020 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.
