Philips recalls a specific model of patient monitor (VM1SpO2, C02, Rec, model 863266) due to unintended distribution and lack of manufacturing records. Affected units may not be intended for commercial use.
Philips has identified a Philips SureSigns VM1 monitor in the possession of a clinical user that was not intended for commercial distribution and for which Philips does not have records regarding its manufacture. Philips is therefore removing this device from distribution.
Philips is recalling a specific patient monitor model because it was distributed without proper records and wasn't intended for commercial use. This means the device might not be safe for regular clinical use.
The device was distributed without being intended for commercial use and Philips lacks records about its manufacture. This means the monitor may not meet safety standards for clinical environments.
Healthcare providers who own or use the Philips SureSigns VM1 monitor model 863266 are likely affected. Clinical users who received this device without proper documentation are at risk.
Check for the model number 863266 on the device. The serial number USPP000004 indicates it was distributed without proper records.
Look for the model number 863266 on the monitor to confirm it is affected.
Philips identified that this specific model was distributed without being intended for commercial use and lacks manufacturing records.
The recall does not provide a fix; Philips is removing the device from distribution.
Check for the model number 863266 and the serial number USPP000004 on the device.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2337-2020 — Philips Philips Hello, I own a Philips that is covered by recall Z-2337-2020 from Philips. 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.
