Medline recalls procedural kits with specific pack numbers due to leaks and breakage risks that could harm patients. Affected kits include arthrograms, circumcision trays, and syringes. Contact Medline for details.
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 specific procedural kits that contain syringes prone to leaks and breakage, which could pose health risks to patients. This recall affects medical kits used in procedures like circumcision and arthrograms.
The kits contain plastic syringes that can leak or break, potentially causing patient health risks. This issue was identified through FDA safety alerts and quality checks.
Healthcare providers and medical facilities using the recalled kits are most at risk. Patients using these kits during procedures may face health issues if the kits leak or break.
Check for pack numbers: SPEC0300B (for arthrograms), CIT6780 (for circumcision trays), CIT4845 (for nursery circumcision trays), MNS9865 (for ultrasound catheter insertion), and DYNDA2497 (for syringes). The kits were sold with specific lot numbers from 2022.
Identify the pack number on the kit to see if it matches the recalled numbers: SPEC0300B, CIT6780, CIT4845, MNS9865, or DYNDA2497.
The recall indicates potential leaks and breakage risks, so they should not be used until the remedy is applied.
Check the pack numbers to confirm if your kits are affected; contact Medline for further instructions.
The recall record does not specify a replacement process or remedy.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2758-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2758-2024 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.
