Medline recalls convenience kits containing specific 10mL polycarbonate syringes with unapproved design changes that may not meet FDA safety standards.
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 outside of FDA 510(k) clearance. This means they might not meet safety standards for medical use, potentially causing issues during procedures like injections or surgeries.
Healthcare professionals using Medline convenience kits with specific syringe models and lots are affected. Those handling the recalled syringes in medical procedures are at the highest risk.
Check for syringes labeled BARIATRIC DYNJ905153M, DYNJ905153N, DYNJ905157K, DYNJ905157L, DYNJ905160O, or DYNJ81602, DYNJ46675G, DYNJ81607, DYNJ905157K, DYNJ905157L, DYNJ905160O, DYNJ81599. Look for specific lot numbers like 24CMG485, 25DMC254, 24ABP080, etc.
Identify if your Medline convenience kit includes the specific syringe models and lot numbers listed in the recall notice.
The recall is due to unapproved design changes to the syringes outside of FDA 510(k) clearance, which may not meet safety standards.
The recall notice does not specify a remedy, so you should check the product details to see if it's affected and contact Medline for further instructions.
Yes, avoid syringes with lot numbers like 24CMG485, 25DMC254, 24ABP080, 24DMF349, 24EMC297, 24FMD083, 24HMD400, 24IME332, 24JMA234, 24KMG588, 25AMA393, 25AMJ541, 25BMI202, 25CMD909, 25CMH371, etc.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1881-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1881-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
