Medline recalls convenience kits with potentially weak breather pouch seals that could lead to contamination during medical procedures. Affected kits include Neuro Pack WRO-LF and Stimulation Implant packs. Consumers should check model numbers and lot dates for affected items.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling several convenience kits used in medical procedures because the breather pouches might have weak seals. This could allow contamination during surgery or other procedures, making the kits unsafe for use.
The breather pouches used to package the sterile kits may have open or weak seals. This could allow contaminants to enter the kit during use, increasing the risk of infection or contamination in medical procedures.
Healthcare professionals using Medline convenience kits for medical procedures are most at risk. Patients undergoing surgeries or treatments with these kits could be exposed to contamination.
Check for model numbers DYNJ41856C, DYNJ53032C, DYNJ50629M, DYNJ40040C, or DYNJ53032C on the kit packaging. Look for lot numbers 24JBM711, 24JBN788, 24JBW674, 24KBC507, or 24KBC655.
Look for model numbers DYNJ41856C, DYNJ53032C, DYNJ50629M, DYNJ40040C, or DYNJ53032C on the kit packaging.
Check if the lot number matches 24JBM711, 24JBN788, 24JBW674, 24KBC507, or 24KBC655.
The breather pouches used to package the sterile kits may have open or weak seals, which could allow contaminants to enter during medical procedures.
Check the model number and lot number on the kit packaging. If it matches the affected items listed, stop using it and contact Medline for instructions.
Yes, weak seals could lead to contamination during medical procedures, increasing the risk of infection or other complications.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1610-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1610-2025 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.
