Cardinal Health recalls IV Start Kits (CATALOG #01-5798B) due to a manufacturing defect causing potential fluid leaks. Affected units include specific lot numbers and expiration dates. Consumers should check their kit's details and follow official instructions.
Presource Kits contains the ICU MicroClave Clear Connector due to a manufacturing defect there is a gap between the connectors top and bottom housings which may lead to fluid leaks and loss of fluid path integrity
Cardinal Health is recalling IV Start Kits with a specific catalog number because a manufacturing defect may cause fluid leaks. This could lead to loss of fluid path integrity, which is important for safe medical use.
The kits contain a gap between the top and bottom housings of the ICU MicroClave Clear Connector due to a manufacturing defect. This gap can cause fluid leaks and loss of fluid path integrity, which may affect medical treatments.
Healthcare professionals and patients using IV Start Kits with the catalog number 01-5798B are likely affected. Those using the kits in medical settings are at higher risk due to the potential for fluid leaks.
Check for the catalog number 01-5798B on the kit. The affected units have specific lot numbers (816643) and expire on February 1, 2025.
Look for the catalog number 01-5798B and lot number 816643 on the kit.
The catalog number is 01-5798B.
The affected lot number is 816643.
The kit expires on February 1, 2025.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1157-2023 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1157-2023 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.