Philips recalls specific Allura 15-12 and related MRI systems due to potential cable hose detachment causing injury. Affected units have serial numbers starting with 722016-722044.
Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or bolts) which May Result in Parts Falling and/or Part of the Cable Hose Dropping, and result in injury.
Philips is recalling several MRI systems that could have broken plastic or bolts causing parts to fall and potentially injure users. This is a safety issue that requires immediate attention to prevent injury.
The cable hose carrier may break due to damaged plastic or loose bolts, causing parts to fall or the cable hose to drop. This could lead to injuries if it strikes a person during medical procedures.
Medical facilities using the recalled Philips Allura 15-12 and related MRI systems are most at risk. Patients and staff during imaging procedures could be affected if the cable hose detaches.
Check for serial numbers starting with 722016 through 722044 on the product labels. The affected models include Allura 15-12, Allura 9, and related MRI systems.
Look for serial numbers starting with 722016 through 722044 on the product labels.
The affected models include Philips Allura 15-12 (722044), Allura 9 (722021 and 722018), and related MRI systems with serial numbers starting with 722016-722044.
The recall is due to potential detachment of the cable hose carrier caused by broken plastic or loose bolts, which could result in parts falling and causing injury.
Check if your serial number starts with 722016 through 722044. If so, contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-3167-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-3167-2024 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.
