Baxter Healthcare recalls certain Automated Peritoneal Dialysis Systems due to improper electrical safety testing. Affected units may have safety risks requiring immediate attention.
The electrical safety testing was not properly performed on the impacted devices and additional testing is required
Baxter Healthcare is recalling specific models of Automated Peritoneal Dialysis Systems because electrical safety testing was not properly performed. This could lead to potential safety issues if the device is used without proper testing.
The recall states that electrical safety testing was not properly performed on the impacted devices. This means the devices might not meet safety standards, potentially causing electrical hazards if used without additional testing.
Patients using Baxter's Automated Peritoneal Dialysis Systems with the listed serial numbers are affected. Those with the specific product codes and serial numbers mentioned in the recall are most at risk.
Check for the product code 5C6M40 and serial numbers listed in the recall: 2010013403, 2102050403, 2103016303, 2103061703, 2104009103, 2105007803, 2105022503, 2110006603, 2110034803, 2111034103, 2202044303, 2203059903, 2203071803, 2203073003, 2204078503, 2203109603.
Verify your device's product code (5C6M40) and serial number against the list provided in the recall.
The electrical safety testing was not properly performed on the impacted devices, requiring additional testing to ensure safety.
The recall does not specify a remedy, so check the product details to see if it is affected and contact Baxter Healthcare for further instructions.
Check for the product code 5C6M40 and serial numbers listed in the recall: 2010013403, 2102050403, 2103016303, 2103061703, 2104009103, 2105007803, 2105022503, 2110006603, 2110034803, 2111034103, 2202044303, 2203059903, 2203071803, 2203073003, 2204078503, 2203109603.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1316-2023 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-1316-2023 from Baxter Healthcare. 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.
