Drs Vascular recalls Q-Stop Suture Retention Devices due to potential inadequate hemostasis during venous access procedures. Affected units include specific model and lot codes.
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Drs Vascular is recalling Q-Stop Suture Retention Devices because they may not properly stop bleeding during medical procedures. This could lead to complications if the device fails to maintain hemostasis.
The device may fail to maintain hemostasis during venous access procedures, potentially leading to uncontrolled bleeding. This risk arises from the device's design and function in managing bleeding after needle insertion.
Medical professionals using the Q-Stop device for venous access procedures are most at risk. Patients undergoing such procedures with the recalled device could experience bleeding complications.
Check for the model number QS on the device packaging or label. Affected units include lot code 00860011629405 (6-pack) and unit of use 10860011629402.
Look for lot code 00860011629405 on the packaging or device label.
The recall indicates a potential risk of inadequate hemostasis, so it is not recommended for use until the remedy is applied.
Check the lot code on the packaging or device label. If it matches 00860011629405, contact Drs Vascular for instructions.
The affected units have lot code 00860011629405 (6-pack) and unit of use 10860011629402. Check the label for these identifiers.
We’ve drafted a message you can send Q-Stop to request your refund or repair — edit it as you like.
Subject: Recall Z-2330-2025 — Q-Stop Q-Stop Hello, I own a Q-Stop that is covered by recall Z-2330-2025 from Q-Stop. 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.
