Philips recalls BrightView XCT gamma cameras for SPECT due to risk of detector falling, potentially causing injuries to lower limbs. Affected models include 6-digit serial numbers starting with 882482 and 12-digit numbers 453560462131 and 453560749161.
Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation.
Philips is recalling BrightView XCT gamma cameras for SPECT because a component failure can cause the detector to fall unexpectedly. If the detector falls below the center of the gantry, it may injure the patient's lower limbs or disrupt system operation. This recall affects specific model numbers.
The detector may fall due to a component failure. If positioned below the center of the gantry, it can cause injuries like lacerations or fractures to the patient's lower limbs. If positioned above the center, it may disrupt system operation but not cause direct injury.
Medical facilities using Philips BrightView XCT gamma cameras for SPECT are likely affected. Patients undergoing scans with these cameras could be at risk if the detector falls.
Check for 6-digit model numbers starting with 882482 or 12-digit numbers 453560462131 and 453560749161. All serial numbers are affected, but no unique identifiers are available for this product.
Verify your camera's model number against the affected numbers: 6-digit format starting with 882482 or 12-digit numbers 453560462131 and 453560749161.
The detector may unexpectedly fall due to a component failure, potentially causing injuries to the patient's lower limbs if positioned below the center of the gantry.
Check your model number against the affected numbers. If it matches, contact Philips for guidance on next steps.
Yes, if the detector falls below the center of the gantry, it can cause lacerations, fractures, or contusions to the patient's lower limbs.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0931-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-0931-2024 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.
