Medline recalls two surgical kits due to incorrect needle and suture sizes in some packages. Affected kits have specific model numbers and expiration dates. Consumers should check their kits and contact Medline for details.
Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.
Medline is recalling two types of surgical kits: the Open Heart CDS (REF CDS840132O) and Dr. Davies CV (REF DYNJ903016G). Some packages contain the wrong needle size or suture length, which could lead to improper wound closure during surgery.
The kits contain suture packages with the wrong needle type, size, or suture diameter and length. This could result in improper wound closure during surgery if the incorrect suture is used.
Healthcare professionals using these kits for procedures are most at risk. Patients receiving surgery with these kits may experience complications if the incorrect suture size is used.
Check for model numbers: CDS840132O (Open Heart CDS) or DYNJ903016G (Dr. Davies CV). Kits were sold with specific lot numbers and expiration dates listed in the recall notice.
Look for the model number on the kit packaging: CDS840132O for Open Heart CDS or DYNJ903016G for Dr. Davies CV.
Reach out to Medline directly to confirm if your kit is affected and get instructions for next steps.
The recall states that some packages contain incorrect suture sizes, so they may not be safe for use without verification.
Check the model number and contact Medline to determine if your kit is affected and follow their instructions.
Look for model numbers CDS840132O or DYNJ903016G on the packaging, and check the lot numbers and expiration dates provided in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0532-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0532-2025 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.
