Medline recalls syringes with potential leaks, breakage, and quality issues that may harm patients. Affected models include 10ml and 20ml syringes with specific item numbers and lot ranges.
These syringes were identified to be affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and other quality issues have been identified that may pose a risk to patient health.
Medline is recalling certain syringes that may leak, break, or have quality issues, which could pose a risk to patient health. These syringes were identified by the FDA in a safety alert from March 19, 2024.
The syringes have been identified by the FDA as having leaks, breakage, and other quality issues that could lead to patient health risks. These problems may occur during normal use, potentially causing harm if the syringe fails during injection.
Users of these syringes for medical purposes are affected. Patients receiving injections with these syringes may be at risk due to potential leaks or breakage.
Check for syringes labeled as SYR 10ML L/L CONTROL (item numbers DNSC91881 or DYNJSYRPPC10) or SYRINGE 20ML BLUE L/L LOW PR (item number DYNJSYRPP20B), among other specific models listed in the recall notice.
Look for the specific product labels and item numbers listed in the recall notice to determine if your syringe is affected.
The FDA identified leaks, breakage, and quality issues in these syringes that could pose a risk to patient health.
Check the label for specific product names and item numbers listed in the recall notice, such as SYR 10ML L/L CONTROL (item numbers DNSC91881 or DYNJSYRPPC10) or SYRINGE 20ML BLUE L/L LOW PR (item number DYNJSYRPP20B).
The recall notice does not specify a remedy, so you should check with Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1936-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-1936-2024 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.