Philips CombiDiagnost R90 1.1 Recall: RF Viewer Shows Previous Patient Images
Philips recalls CombiDiagnost R90 1.1 (709031) models where RF viewer may display previous patient radiography images during fluoroscopy, causing image differences. Affected units have specific serial numbers.
Lower-risk recall
While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.
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What happened, in plain English
Philips is recalling CombiDiagnost R90 1.1 (709031) models where the RF viewer might show previous patient radiography images during fluoroscopy exams. This could cause differences in image content, format, and size. While not dangerous, it may lead to confusion in medical imaging. Read more at govinfonow.com/recall/61155-philips-combidiagnost-r90-1-1-recall-rf-viewer-shows-previous.
Source Summary by GovInfoNow · govinfonow.com/recall/61155-philips-combidiagnost-r90-1-1-recall-rf-viewer-shows-previous · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1088-2024
Cite this page
“Philips CombiDiagnost R90 1.1 Recall: RF Viewer Shows Previous Patient Images.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61155-philips-combidiagnost-r90-1-1-recall-rf-viewer-shows-previous. Based on FDA recall #Z-1088-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1088-2024%22&limit=1).
Why it’s dangerous
During fluoroscopy exams, the RF viewer may display images from previous patients instead of the current patient. This causes differences in image content, format, and size, potentially leading to confusion in medical imaging.
Who’s affected
Healthcare facilities using the CombiDiagnost R90 1.1 (709031) model with specific serial numbers. Medical staff performing fluoroscopy exams are most at risk of image confusion.
How to tell if you have this one
Check if your CombiDiagnost R90 1.1 (709031) has serial numbers listed in the recall (e.g., 10001004 to 10001152). The software version is 1.1.1 or higher.
- Brand
Philips- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution in the states of CA, FL, GA, IL, IN, KS, MD, ME, MI, MN, NC, NJ, NY, TX, VA, WA.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1087-2024 | CombiDiagnost R90 1.0 (709030); Model: R90 1.0 (709030); UDI DI: 00884838076747; Software version 1.1.1 or higher; Serial numbers: 10000000, 10000002, 10000003, 10000004, 10000006, 10000011, 10000012, 10000020, 10000024, 10000027, 10000049, 10000050, 10000065, 10000066, 10000067, 10000069, 10000078, 10000081, 10000099, 10000103, 10000107, 10000140, 10000145, 10000152, 10000180, 10001001, 10001010, 10001095, 591362, SN16000009, SN17000003, SN17000007, SN17000015, SN17000022, SN17000111, SN17000114, SN17000118, SN17000120, SN17000121, SN17000122, SN17000123, SN17000128, SN17000129, SN17000130, SN17000145, SN17000146, SN17000147, SN17000148, SN17000153, SN17000157, SN17000163, SN17000165, SN17000166, SN18000003, SN18000004, SN18000010, SN18000021, SN18000025, SN18000033, SN18000037, SN18000038, SN18000044, SN18000045, SN18000053, SN18000054, SN18000057, SN18000060, SN18000068, SN18000069, SN18000079, SN19000004, SN19000006, SN19000011, SN19000020, SN19000034, SN19000036, 27, 40, 41, 42, 77, 101, 131, 155, 180, 190; | 86 units |
| Z-1088-2024 | CombiDiagnost R90 1.1 (709031); Model: R90 1.1 (709031); UDI DI: 00884838101456; Software version 1.1.1 or higher; Serial Numbers: 10001004, 10001005, 10001006, 10001008, 10001009, 10001010, 10001011, 10001012, 10001013, 10001018, 10001020, 10001022, 10001024, 10001026, 10001027, 10001028, 10001029, 10001030, 10001031, 10001032, 10001035, 10001036, 10001043, 10001044, 10001045, 10001046, 10001047, 10001048, 10001049, 10001050, 10001051, 10001052, 10001053, 10001054, 10001055, 10001056, 10001057, 10001058, 10001059, 10001060, 10001061, 10001062, 10001063, 10001064, 10001065, 10001066, 10001067, 10001068, 10001069, 10001070, 10001071, 10001072, 10001073, 10001074, 10001075, 10001076, 10001077, 10001078, 10001079, 10001080, 10001081, 10001083, 10001084, 10001085, 10001086, 10001087, 10001088, 10001089, 10001090, 10001091, 10001092, 10001093, 10001094, 10001095, 10001096, 10001097, 10001098, 10001099, 10001100, 10001101, 10001102, 10001103, 10001104, 10001105, 10001106, 10001107, 10001108, 10001109, 10001110, 10001111, 10001112, 10001113, 10001114, 10001115, 10001116, 10001117, 10001118, 10001119, 10001120, 10001121, 10001122, 10001123, 10001124, 10001125, 10001126, 10001127, 10001128, 10001129, 10001130, 10001131, 10001132, 10001133, 10001134, 10001135, 10001136, 10001137, 10001138, 10001139, 10001140, 10001141, 10001142, 10001143, 10001144, 10001145, 10001147, 10001148, 10001149, 10001150, 10001152, 10001201; | 130 units |
What to do — step by step
Check Device Serial Number
Verify your CombiDiagnost R90 1.1 (709031) has a serial number from the list provided in the recall.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 16 states.
FDA distribution: “US Nationwide distribution in the states of CA, FL, GA, IL, IN, KS, MD, ME, MI, MN, NC, NJ, NY, TX, VA, WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Florida, Georgia, Illinois, Indiana, Kansas, Maine, Maryland, Michigan, Minnesota, New Jersey, New York, North Carolina, Texas, Virginia, Washington.
Recall timeline
FDA published this recall 2 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if my device is affected?
The recall does not require immediate action. Affected units may be monitored for image differences during use.
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Where this comes from
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.
- Official source: FDA Recall #Z-1088-2024 (February 11, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1088-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.