Medline recalls convenience kits containing unapproved 10mL polycarbonate syringes that may not meet safety standards. Affected kits include ARTHROSCOPY PACK DYNJ451: 10889942485222 (EA) and 40889942485223 (CS) from lot 24BBB811.
Unapproved design changes to the products outside of the 510(k) clearance.
Medline is recalling convenience kits that include certain 10mL polycarbonate syringes due to unapproved design changes not cleared by the FDA. This could mean the syringes don't meet safety standards and might pose risks during medical use.
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, potentially causing issues during procedures.
Healthcare professionals using Medline Convenience Kits with the specific syringe models listed in the recall. Those handling the kits in medical settings are most at risk.
Check for the ARTHROSCOPY PACK DYNJ45173D label on the convenience kit. The syringes have unique identifiers: 10889942485222 (EA) and 40889942485223 (CS) from lot 24BBB811.
Look for the ARTHROSCOPY PACK DYNJ45173D label and the specific syringe identifiers listed in the recall.
The syringes have unapproved design changes not cleared by the FDA through the 510(k) process, which may mean they don't meet safety standards.
The recall record does not specify a remedy, so there is no action required beyond checking if you have the affected items.
Check for the ARTHROSCOPY PACK DYNJ45173D label and the syringe identifiers: 10889942485222 (EA) and 40889942485223 (CS) from lot 24BBB811.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1888-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1888-2026 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.
