Baxter recalls CAPD MiniCap Transfer Set (34cm) due to risk of leaks or cracks from cleaning products like bleach or hydrogen peroxide.
Cleaning products, containing, but not limited to, hydrogen peroxide, bleach, alcohol, or antiseptic agents and solvent, such as those containing acetone, toluene, xylene, or cyclohexanone may cause damage, such as leaking or cracking, to the MiniCap Extended Life PD transfer sets.
Baxter is recalling its CAPD MiniCap Transfer Set (34cm) because certain cleaning products can damage the product, causing leaks or cracks. This affects healthcare workers using the device for patient care.
Cleaning products containing hydrogen peroxide, bleach, alcohol, or solvents like acetone can damage the transfer set's material. This may lead to leaks or cracks, potentially affecting patient care.
Healthcare workers using Baxter's CAPD MiniCap Transfer Set for patient care are most at risk. The recall applies to all units sold with the specific model and code.
Check for the model name 'CAPD MiniCap Transfer Set II (34cm)' and code number T5C4484. The recall covers all units within the product's expiry date.
Identify the model name and code number on the product to confirm if it's affected.
Cleaning products like hydrogen peroxide, bleach, or solvents can cause leaks or cracks in the transfer set.
Check the product details to see if it's affected; the recall covers all units within the product's expiry date.
The recall does not provide a fix; affected units should be checked for damage before use.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0580-2022 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0580-2022 from Baxter. 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.