Medline recalls procedure kits with plastic syringes that may leak or break, posing health risks. Affected kits have specific pack numbers and lot numbers. Consumers should check their kits for these identifiers.
Medical convenience kits contain plastic syringes 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 procedure kits that contain plastic syringes which may leak or break, potentially harming patients. These kits were sold with specific pack numbers and lot numbers identified in the recall notice.
The plastic syringes in these kits may leak or break, which could lead to contamination or injury. This poses a risk to patient health as the kits are used in medical procedures.
Healthcare professionals and medical facilities using the recalled procedure kits are most at risk. Patients using these kits could be affected if the kits leak or break.
Check for pack numbers starting with DYNJ followed by 5-7 digits, such as DYNJ57622 or DYNJ48483B. Also look for lot numbers like 20LMF902A or 22CMB584A on the packaging.
Look for pack numbers starting with DYNJ followed by 5-7 digits and lot numbers like 20LMF902A or 22CMB584A on the packaging.
The plastic syringes in these kits may leak or break, potentially causing contamination or injury to patients.
Check for pack numbers starting with DYNJ followed by 5-7 digits, such as DYNJ57622 or DYNJ48483B, and lot numbers like 20LMF902A or 22CMB584A on the packaging.
The recall notice does not specify a remedy, so contact Medline directly to determine next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1448-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1448-2025 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.
