Vascular Solutions recalls Langston Dual Lumen Catheters with specific model numbers due to risk of inner lumen separating from hub during pressure injection. Affected units include lots 643376 to 673021.
The inner lumen of the Langston catheter may separate from the hub during pressure injection.
Vascular Solutions is recalling Langston Dual Lumen Catheters with certain model numbers because the inner lumen may separate from the hub during pressure injection. This could lead to improper fluid delivery or blockages if the catheter is used in medical procedures.
During pressure injection, the inner lumen of the catheter may separate from the hub. This could cause improper fluid delivery, blockages, or potential complications in medical procedures if the catheter is used without the lumen properly connected.
Healthcare professionals using the Langston Dual Lumen Catheter for medical procedures are most at risk. Patients receiving treatment with these catheters may be affected if the device is used improperly.
Check for model numbers 5540, UDI 10841156100513, and lots 643376 through 673021 on the catheter packaging or label. The recall covers specific production lots listed in the official notice.
Identify the model number, UDI, and lot numbers on the catheter to determine if it is affected.
The inner lumen may separate from the hub during pressure injection, which could lead to improper fluid delivery or blockages in medical procedures.
Check the model number, UDI, and lot numbers to see if it is affected. If it is, contact Vascular Solutions for further instructions.
Yes, if the inner lumen separates during pressure injection, it could cause improper fluid delivery or blockages, potentially leading to complications in medical procedures.
We’ve drafted a message you can send Vascular Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-0111-2021 — Vascular Solutions Vascular Solutions Hello, I own a Vascular Solutions that is covered by recall Z-0111-2021 from Vascular Solutions. 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.
