Medline is recalling certain catheterization kits due to potential lack of sterility in solutions, which could lead to infection risks. Affected kits have specific lot numbers and labels.
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Medline is recalling catheterization kits that may contain non-sterile solutions, which could lead to infection risks. This recall affects kits with specific lot numbers and labels.
The recall is due to potential lack of sterility in the solutions (0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP, and Saline Flush Syringe) used in the kits. If the solutions are non-sterile, they could cause infections in patients or healthcare workers.
Healthcare workers and patients using the recalled catheterization kits are at risk of infection if the solutions are non-sterile. The risk is primarily for those using the kits in medical settings.
Check for kits labeled 'CATHETERIZATION KIT, REF DYNDA2939' with lot number 22GBO521. The case number is 40195327132492 and the unit number is 10195327132491.
Look for the label 'CATHETERIZATION KIT, REF DYNDA2939' with lot number 22GBO521 on the case and unit.
The recall is due to potential lack of sterility in the solutions used in the kits, which could lead to infection risks.
Check the kit labels for the specific lot number 22GBO521 and contact Medline for further instructions.
The potential lack of sterility could lead to infection risks, but the recall is for specific kits with the mentioned lot numbers.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1104-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1104-2024 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.
