Maquet recalls Hemopro 2 with Vasoshield Model VH-4001 due to potential ink chip causing patient harm. Affected units have specific serial numbers.
Ink on the Vasoshield syringe Maquet logo may chip resulting in an unreasonable risk of harm to the patient. Potential harms may include foreign body reaction, coronary embolic event, and peripheral embolic event.
Maquet is recalling Hemopro 2 with Vasoshield syringes (Model VH-4001) because ink on the Maquet logo may chip, risking foreign body reactions or blood clots in patients. This could cause serious health issues during medical procedures.
The ink on the syringe's Maquet logo may chip during use, potentially causing small pieces of ink to enter the patient's bloodstream. This could lead to foreign body reactions, blood clots, or blockages in blood vessels.
Healthcare professionals using the Hemopro 2 with Vasoshield syringe Model VH-4001 for medical procedures are most at risk. Patients receiving treatments with these syringes could face complications.
Check for the model number VH-4001 on the syringe. Affected units have specific serial numbers listed in the recall notice, including 25152107 and others.
Look for the model number VH-4001 on the syringe to confirm if it's affected.
Reach out to Maquet Cardiovascular, LLC for guidance on next steps if you have an affected syringe.
The ink on the Maquet logo may chip, potentially causing foreign body reactions or blood clots in patients during medical procedures.
Check the syringe model and serial numbers against the list provided in the recall notice. Contact Maquet Cardiovascular, LLC for further instructions.
Yes, the recall states potential harms include foreign body reactions, coronary embolic events, and peripheral embolic events, which could be serious.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-0995-2023 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-0995-2023 from Maquet. 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.
