Medline recalls convenience kits containing unapproved 10mL polycarbonate syringes with design changes not cleared by FDA. Affected kits have specific model numbers and lots. Consumers should check their kits for listed serial numbers.
Unapproved design changes to the products outside of the 510(k) clearance.
Medline is recalling convenience kits that include certain 10mL polycarbonate colored syringes due to unapproved design changes not cleared by the FDA. This recall affects kits with specific model numbers and production lots listed in the notice.
The syringes have unapproved design changes that were not cleared by the FDA through the 510(k) process. This means the products may not meet safety standards and could pose risks if used improperly.
People who own or use Medline Convenience Kits containing the specified syringes with model numbers DYNJ908706D or DYNJ909398A and production lots listed in the recall notice are affected. Healthcare professionals and medical facilities using these kits are most at risk.
Check your Medline Convenience Kits for model numbers DYNJ908706D or DYNJ909398A and production lots listed in the recall notice, such as 24GMH510, 24HMG886, or 23EMF078.
Identify your Medline Convenience Kit model number and production lot from the recall list.
The syringes have unapproved design changes not cleared by the FDA through the 510(k) process.
Model numbers DYNJ908706D and DYNJ909398A with specific production lots listed in the recall notice.
The recall does not specify a stop-use action; the remedy is null, so users should check if their kits are affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1885-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1885-2026 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.
