Medline recalls convenience kits containing unapproved 10mL polycarbonate syringes that were made without proper regulatory clearance.
Unapproved design changes to the products outside of the 510(k) clearance.
Medline is recalling convenience kits that include certain 10mL polycarbonate colored syringes because they were made with design changes not approved by regulators. This could lead to safety issues if the syringes are used without proper clearance.
The syringes were made with design changes that were not approved by regulatory authorities. This means they might not meet safety standards, potentially causing issues during medical use.
Healthcare workers and others who use these syringes in medical settings may be affected. Those using the recalled kits are most at risk.
Check for the model number DYNJ0373061J on the syringes. The kits were sold with specific lot numbers and dates, including lot 24ABR895.
Look for the model number DYNJ0373061J on the syringes and the lot number 24ABR895 on the packaging.
The syringes were made with design changes not approved by regulatory authorities, which could lead to safety issues.
The official recall notice does not specify a remedy or action for affected users.
Yes, the lot number 24ABR895 is associated with the recalled kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1889-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1889-2026 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.
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