Cardinal Health recalls Presource kits and trays with specific catalog numbers due to potential patient harm from defective syringes. The syringes may cause inaccurate dosing or leaking.
Cardinal Health is following the FDA's recommendations regarding the disposition of affected Jiangsu Shenli Medical Production Co. Ltd (Shenli) Syringes in the Merit Medical¿ supplied finished kits. Merit Medical¿ supplied finished kits are included as components in Presource kits. According to the FDA s communication, these Shenli syringes, located inside a Merit Medical¿ kit component, cannot be distributed for use as they could contain a significant change or modification in design which could significantly alter the safety or effectiveness of the finished kit product, resulting in the risk of patient harm such as inaccurate dosing and a leaking device.
Cardinal Health is recalling Presource kits and trays that contain syringes from a Chinese manufacturer. These syringes could lead to inaccurate dosing or leaking during medical procedures, risking patient harm.
The syringes inside the kits were made by a Chinese manufacturer that may have altered the design, potentially causing inaccurate dosing or leaking during medical procedures. This could lead to patient harm.
Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving treatments with these kits could face inaccurate dosing or leaking devices.
Check for Presource kits and trays labeled with catalog numbers starting with SAN13BS605 through SAN73CHSJK. Look for specific lot numbers listed in the recall notice.
Look for catalog numbers starting with SAN13BS605 through SAN73CHSJK on the product labels.
Contact Cardinal Health directly for more information about the recall and to confirm if your product is affected.
Cardinal Health is recalling these kits because the syringes inside them were made by a Chinese manufacturer that may have altered the design, potentially causing inaccurate dosing or leaking during medical procedures.
Check the product labels for the catalog numbers listed in the recall notice. Contact Cardinal Health to confirm if your product is affected.
Yes, the syringes could cause inaccurate dosing or leaking during medical procedures, which may lead to patient harm.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2327-2024 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2327-2024 from Cardinal Health. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.