Merit Medical recalls Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F (REF 49922: Version A) due to valve failure preventing fluid drainage. Affected units have specific lot numbers.
There is a potential that valve assemblies will not open. preventing fluid from draining.
Merit Medical is recalling Aspira Peritoneal Drainage Catheter Insertion Trays because valve assemblies might not open, preventing fluid drainage. This could lead to complications if the drainage system isn't working properly.
The valve assemblies in the tray might not open properly, which can prevent fluid from draining. This could lead to complications such as fluid buildup or infection if the drainage system isn't functioning correctly.
Healthcare professionals using the Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F for medical procedures are most at risk. Patients receiving this device may also be affected if the drainage system fails.
Check for the product name 'Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F', reference number 4992208, Version A, and sterile packaging. Lot numbers I2538438, I2614180, or I2623234 are affected.
Identify the product name, reference number, version, and lot numbers to confirm if your item is affected.
The recall states there is a potential that valve assemblies will not open, preventing fluid drainage. This could lead to complications, so affected units should be checked.
The recall does not specify a remedy, so check the product details to confirm if it's affected and contact Merit Medical for further instructions.
Look for the product name 'Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F', reference number 4992208, Version A, and lot numbers I2538438, I2614180, or I2623234.
We’ve drafted a message you can send Merit Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1910-2023 — Merit Medical Systems Merit Medical Systems Hello, I own a Merit Medical Systems that is covered by recall Z-1910-2023 from Merit Medical Systems. 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.
