Baxter recalls MiniCap Extended Life PD Transfer Sets with REF R5C4483 that may leak or crack when exposed to 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 MiniCap Extended Life PD Transfer Sets with REF R5C4483 because cleaning products such as bleach or hydrogen peroxide can cause leaks or cracks. This poses a risk of contamination or damage to medical equipment.
Cleaning products containing hydrogen peroxide, bleach, alcohol, or solvents like acetone can damage the MiniCap sets by causing leaks or cracks. This could lead to contamination or improper function of the medical device.
Patients using these transfer sets for medical procedures may be affected if cleaning products damage the device. Healthcare workers handling the sets are most at risk.
Check for the product name 'Baxter MiniCap Extended Life PD Transfer Set Twist Clamp - Extra Short' and reference number R5C4483. The recall covers all units within the expiry date.
Look for the reference number R5C4483 on the device or packaging.
Cleaning products like bleach or hydrogen peroxide may cause leaks or cracks in the MiniCap sets.
The recall covers all units with reference number R5C4483 within the expiry date. Check the product details to confirm.
The recall does not mention serious injury risks; the hazard is limited to potential leaks or cracks from cleaning products.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0577-2022 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0577-2022 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.
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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.
