Medline is recalling serum tear kits with specific lot numbers due to potential non-sterile solutions. This could cause infection if used improperly. Affected kits have labels including 'SERUM TEAR KIT, REF DYNDA154: 22FMC728 or 23CMB090 lots.
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 serum tear kits that may contain non-sterile solutions, which could lead to infections if used. This recall affects kits with specific lot numbers and labels.
The kits were manufactured using specific lots of Nurse Assist components that may not be sterile. If the solution is non-sterile, it could cause infections when used for medical purposes.
Healthcare workers and patients using the serum tear kits with the specified lot numbers and labels are most at risk. The recall targets specific kits sold under the 'SERUM TEAR KIT, REF DENYDA1545' label.
Check for kits labeled 'SERUM TEAR KIT, REF DYNDA1545' with case lot numbers 22FMC728 or 23CMB090. The units have lot numbers 10889942214884.
Look for the label 'SERUM TEAR KIT, REF DYNDA1545' with case lot numbers 22FMC728 or 23CMB090.
The recall is due to potential lack of sterility in the solution, which could cause infections if used.
Case lot numbers 22FMC728 and 23CMB090; unit lot number 10889942214884.
Check for the label 'SERUM TEAR KIT, REF DYNDA1545' with the specific case and unit lot numbers listed.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1100-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1100-2024 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.
