Medline recalls blood draw kits with specific lot numbers due to potential non-sterile solutions from contaminated components. Affected kits may cause infection if used improperly.
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 certain blood draw kits and lab collection kits that used contaminated components. Using these kits could lead to infections if the solutions are not sterile.
The kits were manufactured using specific lots of Nurse Assist components that could be non-sterile. This means the solutions might not be safe for medical use, potentially causing infections.
Healthcare workers and patients using the recalled kits may be at risk of infection. Those with the specific lot numbers listed are most affected.
Check the kit labels for the model numbers: DYNDV2183A, DYNDH1641A, DYNDH1641AH, or DYNDH1719A. Look for lot numbers like 22ABT635, 22ABY152, or 23ABC589.
Look for model numbers and lot numbers on the kit packaging to determine if it's affected.
Reach out to Medline for guidance on next steps if you have the affected kits.
Medline issued a recall because the kits used components that could be non-sterile, posing a risk of infection.
Blood draw kits with model numbers DYNDV2183A, DYNDH1641A, DYNDH1641AH, or DYNDH1719A and specific lot numbers.
Check the kit label for the model number and lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1115-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1115-2024 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.
