Baxter recalls ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Sets due to customer reports of tubing separation from the Male Luer Lock Adaptor. Affected units have specific lot numbers and expiration dates.
There were customer reports of separation between the tubing and Male Luer Lock Adaptor.
Baxter is recalling ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Sets after customer reports of tubing separating from the Male Luer Lock Adaptor. This could lead to improper IV connections and potential complications during medical treatment.
The tubing may separate from the Male Luer Lock Adaptor during use, which could cause improper IV connections. This might lead to medication errors or infection risks if the connection is not secure.
Healthcare professionals and patients using Baxter ONE-LINK catheter extension sets for IV treatments are affected. Those with the specific lot numbers listed in the recall are at risk.
Check for the product name 'Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set' with lot numbers DR18E01023, DR18E07053, DR19G08023, DR19H07015, DR19L09030, or DR20B04020. The expiration dates range from May 2, 2023 to February 5, 2025.
Verify the lot number and expiration date on the product label to confirm if it is affected.
If you have the affected product, contact your healthcare provider for guidance on next steps.
Baxter recalls this product due to customer reports of tubing separating from the Male Luer Lock Adaptor, which could cause improper IV connections.
Affected lot numbers include DR18E01023 (exp. 5/2/2023), DR18E07053 (exp. 5/8/2023), DR19G08023 (exp. 7/8/2024), DR19H07015 (exp. 8/7/2024), DR19L09030 (exp. 12/10/2024), and DR20B04020 (exp. 2/5/2025).
The recall record does not specify a fix or remedy for this issue.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1102-2021 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1102-2021 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.
