Philips North America Llc recalls Spectral CT. Computed tomography X-ray system.
Devices with affected software may experience two unintended motion issues that may lead to contact between the Gantry or table with the operator or patient, along with additional software issues that affect CT…
Read the official notice →- Date
- 2025-07-02
- Country
- United States
- Brand
- Philips
- Product
- Spectral CT. Computed tomography X-ray system.
- Classification
- Class II
- Units
- Domestic: AZ, CA, CO, FL, GA, HI, IN, KY, MA, MD, MN, NY, OH, OR, PA, TX, VT,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Philips recalls
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Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.
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The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice → - 2025-08-06
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FDA · DevicePhilips North AmericaWorldwide distribution - US Nationwide and the countries of Albania, Algeria,…Official notice → - 2025-06-18
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identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the…
FDA · DevicePhilips North AmericaWorldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI,…Official notice → - 2025-05-28
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FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Andorra,…Official notice → - 2025-05-14
- US
Philips North America Llc recalls Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm…
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FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of AE, AL, AO, AR,…Official notice →
Other drugs & medical recalls in the United States
- 2025-07-09
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Church & Dwight Inc recalls Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL), NET 0.08 FL OZ (2.6 mL) TOTAL, 12 Single-Use Swabs per carton,…
Microbial Contamination of Non-Sterile Products: Fungal contamination of infant oral swabs.
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Church & Dwight Inc recalls ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216…
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Tailstorm Health INC recalls KETAmine Hydrochloride Injection, USP, 50 mg/5mL (10 mg/mL), For IM Use or Slow IV Use, 5 mL Sterile Single-Dose Vial, Rx Only, For Office…
Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.
- 2025-07-02
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Jewel Precision Sheet Metal & Machining Co, Inc. recalls Jewel Precision Reusable Rigid Sterilization Container System. Model Number: JP-24-8.
The 8-inch model of the Jewel Precision Reusable Rigid Sterilization Container System (i.e., model number: JP-24-8) was not cleared by the FDA. The letter to file justifying the change in size was insufficient.
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