Medline recalls two specific circumcision trays (CIT6780 and CIT6920) due to leaks and breakage risks that could harm patients. Affected units include those with specific lot numbers sold in 2022-2023.
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 two types of circumcision trays because they may leak or break, posing a risk to patient health. This is a safety issue that requires immediate attention to prevent harm.
These trays contain plastic syringes that can leak or break, which may lead to patient health risks. The issue stems from quality problems identified in the FDA Safety Alert from March 2024.
Healthcare providers using Medline circumcision trays with specific pack numbers and lot numbers from 2022-2023 are affected. Patients receiving procedures using these trays are at risk of potential health issues.
Check for trays labeled 'MEDICAL CIRCUMCISION TRAY' (Pack Number CIT6780) or 'NICU CIRCUMCISION TRAY W/OUT CLAMP' (Pack Number CIT6920). The lot numbers are 2022072650 for CIT6780 and 2023101290 for CIT6920.
Look for the specific pack numbers and lot numbers listed in the recall notice to confirm if your tray is affected.
The recall indicates potential leaks and breakage risks, so they are not safe to use as described in the FDA Safety Alert.
The recall does not specify a remedy, so you should check the product labels to confirm if it is affected and contact Medline for further guidance.
Check for the specific pack numbers (CIT6780 or CIT6920) and lot numbers (2022072650 or 2023101290) on the tray label.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2744-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2744-2024 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.
