Recall archive / FDA device enforcement
DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic ima... — FDA record Z-0275-2024
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Sep 21, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.
- Reason
- Potential for units suspended on the ceiling to fail and fall.
- Classification
- Class II
- Recalling firm
- Philips North America Llc
- Quantity
- 33 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0275-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Model No. 712035; UDI: (01)00884838090705(21)10000009, (01)00884838090705(21)10000010, (01)00884838090705(21)10000003, (01)00884838090705(21)10000004, (01)00884838090705(21)10000002, (01)00884838090705(21)10000001, (01)00884838090705(21)10000053 , (01)00884838090705(21) 10001042 , (01)00884838090705(21) 10001044 , (01)00884838090705(21) 10001125 , (01)00884838090705(21) 10001113 , (01)00884838090705(21) 10001111 , (01)00884838090705(21) 10001112 , (01)00884838090705(21) 10001109 , (01)00884838090705(21) 10001110 , (01)00884838090705(21) 10001114 , (01)00884838090705(21) 21862107 , (01)00884838090705(21) 10001130 , (01)00884838090705(21) 21862103 , (01)00884838090705(21) 21862101 , (01)00884838090705(21) 21862100 , (01)00884838090705(21) 22860370 , (01)00884838090705(21) 21862123 , (01)00884838090705(21) 21862126 , (01)00884838090705(21) 22860323 , (01)00884838090705(21) 22860045 , (01)00884838090705(21) 22860317 , (01)00884838090705(21) 22860316 , (01)00884838090705(21) 22860318 , (01)00884838090705(21) 22860342 , (01)00884838090705(21) 22860357 , (01)00884838090705(21) 23860320 , (01)00884838090705(21) 23860316; Serial No. 10000009, 10000010, 10000003, 10000004, 10000002, 10000001, 10000053, 10001042, 10001044, 10001125, 10001113, 10001111, 10001112, 10001109, 10001110, 10001114, 21862107, 10001130, 21862103, 21862101, 21862100, 22860370, 21862123, 21862126, 22860323, 22860045, 22860317, 22860316, 22860318, 22860342, 22860357, 23860320, 23860316. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Nationwide distribution.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Nov 15, 2023
- Recall initiation date
- Sep 21, 2023
- Center classification date
- Nov 8, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.