Device recall: Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
Class II FDA enforcement event 99511. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
Potential of failing to trigger clinical scan during Bolus Tracking.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Philips Healthcare (Suzhou) Co., Ltd. started this device recall on 26 Jun 2026. The firm address in the FDA record is in Suzhou. FDA put the recall in Class II. FDA event 99511 has 1 product record. The first FDA enforcement report date is 2 Sep 2026. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
U.S. Nationwide and U.S. Territories distribution.
Recalling firm
Philips Healthcare (Suzhou) Co., Ltd., Suzhou, N/A, China.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: FDA Mandated.
Products
1 product record in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-2988-2026 | Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144. | N/A | Class II | Ongoing | 2 Sep 2026 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2026
- 572
- Share of these events in Class II
- 87%
- Product records in this event
- 1Median of the firm: 1
- Events of the firm on the register
- 4
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 3 Dec 2025 | Philips Incisive CT | Device | Class II | 1 |
| 23 Dec 2022 | Incisive CT, model 728143 & 728144 running Software Version 5.0.0. | Device | Class II | 1 |
| 24 Feb 2021 | Philips CT systems are advanced continuous-rotation computed tomography systems suitable for a wide range of computed to | Device | Class II | 1 |
Official channels
- FDA enforcement report Z-2988-2026The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 99511. https://recallregister.com/fda/ii/99511/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
U.S. Nationwide and U.S. Territories distribution.
- What quantity of product is in FDA event 99511?
- The FDA record gives this quantity:
N/A
- How did the recall start?
- The FDA record says:
FDA Mandated
- How many device recalls of 2026 have the same class?
- 87% of the 572 device events that started in 2026 are in Class II.