Baxter recalls Clearlink Continu-Flo Administration Sets with specific product codes due to potential connection issues that may cause dislodgement during fluid administration.
Continu-Flo sets with male Luer bodies at the lower end of, and within, the ISO specification for outer diameter require a higher than expected connection force to fully inset and securely tighten the Luer to the ONE-LINK connector.
Baxter is recalling Clearlink Continu-Flo Administration Sets with product codes 2C8519, 2C8537, and 2C8541. These sets have a male Luer body that requires higher connection force than expected, which could lead to dislodgement during use.
The male Luer bodies on these sets are designed to fit within a specific ISO outer diameter specification. This requires more force to securely connect to the ONE-LINK connector than intended, increasing the risk of dislodgement during fluid administration.
Healthcare professionals and patients using these specific Clearlink Continu-Flo sets for fluid administration are affected. Those using the sets with the listed product codes are most at risk.
Check for product codes 2C8519, 2C8537, or 2C8541 on the sets. These sets are used for administering fluids into patients' vascular systems.
Look for product codes 2C8519, 2C8537, or 2C8541 on the Clearlink Continu-Flo Administration Sets.
Product codes 2C8519, 2C8537, and 2C8541 are recalled.
The male Luer bodies on these sets require higher connection force than expected, which could lead to dislodgement during fluid administration.
Check the product codes on the sets. If you have the recalled codes, contact Baxter for further instructions.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0793-2020 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0793-2020 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.
