Medline recalls specific medical procedure kits due to slight dimensional variations that could make them harder to fit into outer canisters. Affected kits include nasal, bronchial, ENT, and other surgical kits with listed reference numbers and lot numbers.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling certain medical procedure kits that have a slight size variation which might make them harder to fit into their outer canisters. This could cause issues during medical procedures but does not pose a safety risk to users.
The kits have a slight dimensional variation that could make them harder to fit into their outer canisters. This might cause difficulties during medical procedures but does not involve a risk of injury or damage to the user.
Healthcare professionals using the recalled Medline medical procedure kits are most at risk. Patients using these kits during procedures may also be affected if the kits don't fit properly.
Check the product label for reference numbers like DYNJ909932, DYKE1007B, or DYNJ909935. Look for lot numbers such as 23JBI290, 22HBF709, or 23JBH869 on the packaging.
Look for reference numbers like DYNJ909932, DYKE1007B, or DYNJ909935 on the kit packaging.
No, the recall does not require stopping use immediately. The issue is a slight size variation that may cause fitting difficulties but does not pose a safety risk.
Check the product label for reference numbers like DYNJ909932, DYKE1007B, or DYNJ909935 and lot numbers such as 23JBI290, 22HBF709, or 23JBH869.
The recall does not mention any fix or remedy. Affected kits should be checked and potentially replaced if they are not fitting properly.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2703-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2703-2024 from Medline. 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.
