Medline recalls convenience kits containing specific 10mL polycarbonate syringes due to unapproved design changes. Affected kits may not be safe for medical use without regulatory approval.
Unapproved design changes to the products outside of the 510(k) clearance.
Medline is recalling convenience kits that include certain 10mL polyc:carbonate colored syringes because they have unapproved design changes. This could mean the syringes aren't safe for medical use without proper regulatory approval.
The syringes have unapproved design changes that weren't cleared by the FDA through the 510(k) process. This means they might not meet safety standards for medical use.
Healthcare workers using Medline convenience kits with the specified syringes are most at risk. Patients receiving injections with these syringes could be affected.
Check for the model numbers DYNJ41792G or DYNJ53744B on the syringes. The kits were sold with specific lot numbers like 24ABS765 or 24ABT556.
Look for model numbers DYNJ41792G or DYNJ53744B on the syringes and lot numbers 24ABS765 or 24ABT556.
The syringes have unapproved design changes that weren't cleared by the FDA through the 510(k) process.
The recall record does not specify a remedy, so check with Medline for guidance.
The recall indicates they may not be safe for medical use without regulatory approval.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1892-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1892-2026 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.
