Baxter recalls CLEARLINK System with DUO-VENT Spike (Product Code 2R840:1) due to reported leaks at injection sites. Affected units may cause injury; stop using immediately.
Firm noted an increase in customer reports of leaks.
Baxter is recalling its CLEARLINK System with DUO-VENT Spike due to customer reports of leaks at injection sites. This could lead to injury if the leaks occur during medical use.
Leakage at the injection site can cause contamination or injury to the patient. The leaks are reported by customers but not confirmed to cause serious harm in normal use.
Healthcare providers using the CLEARLINK System with DUO-VENT Spike for injections are most at risk. Patients receiving treatments with this system may also be affected.
Check for the product code 2R8403 on the CLEARLINK System with DUO-VENT Spike. The system was sold with a unique identifier (UDI/DI) 00085412656649 and all lots within expiry.
Discontinue use of the CLEARLINK System with DUO-VENT Spike if leaks are observed at the injection site.
Baxter noted an increase in customer reports of leaks at the injection site.
Stop using it immediately if leaks are observed at the injection site.
The recall does not mention a fix; the remedy is not specified.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1653-2022 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1653-2022 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.
