Wilson-Cook Medical recalls Hemospray Endoscopic Hemostats with model numbers HEMO-10, HEMO-10-EU, H: potential for powder spraying failure due to misassembly.
Potential for Hemospray device to be unable to spray powder due to misassembly of devices.
Wilson-Cook Medical is recalling Hemospray Endoscopic Hemostats with specific model numbers and lot codes because they may not spray powder properly due to manufacturing errors. This could affect medical procedures requiring precise hemostasis.
The device may not spray powder correctly because of improper assembly during manufacturing. This could lead to ineffective hemostasis during medical procedures, potentially causing bleeding that requires additional intervention.
Healthcare professionals using the Hemospray devices for medical procedures are most at risk. Patients receiving these procedures may be affected if the device fails during treatment.
Check for model numbers HEMO-10, HEMO-10-EU, or HEMO-7-EU and lot codes W4179646, W4180858, W4180861, W4181073, W4180860, W4181071, W4189223, or W4189224 on the device packaging or label.
Identify the model number on the device label to confirm if it matches HEMO-10, HEMO-10-EU, or HEMO-7-EU.
Check the lot code on the device packaging to see if it matches the listed codes: W4179646, W4180858, W4180861, W4181073, W4180860, W4181071, W4189223, or W4189224.
The Hemospray devices may not spray powder properly due to manufacturing errors, which could affect medical procedures requiring precise hemostasis.
Model numbers HEMO-10, HEMO-10-EU, and HEMO-7-EU are affected.
Lot codes W4179646, W4180858, W4180861, W4181073, W4180860, W4181071, W4189223, and W4189224 are affected.
We’ve drafted a message you can send Wilson-Cook Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2541-2019 — Wilson-Cook Medical Wilson-Cook Medical Hello, I own a Wilson-Cook Medical that is covered by recall Z-2541-2019 from Wilson-Cook Medical. 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.