Radiometer recalls arterial blood samplers due to potential sterility issues. All units sold may be affected. Consumers should contact Radiometer for details.
Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf life of the product.
Radiometer is recalling arterial blood samplers that may not be sterile throughout their shelf life. This could lead to infections if used improperly.
The blood samplers may not maintain sterility over time, increasing infection risk during medical procedures. This is a potential issue for patients undergoing blood tests.
Healthcare professionals and patients using arterial blood samplers for medical testing. Those with specific medical conditions requiring frequent blood tests are at higher risk.
Check for the model number REF:956-552, PIC050 on the product. The product is sold as an arterial blood sampler with 2 mL capacity and 80 IU heparin.
Reach out to Radiometer Medical ApS for specific instructions on handling the recalled product.
The recall states sterility cannot be guaranteed, so it may not be safe for medical use.
Look for the model number REF:956-552, PIC050 on the product label.
Contact Radiometer Medical ApS for specific instructions on handling the recalled product.
We’ve drafted a message you can send Radiometer to request your refund or repair — edit it as you like.
Subject: Recall Z-1115-2022 — Radiometer Radiometer Hello, I own a Radiometer that is covered by recall Z-1115-2022 from Radiometer. 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.
