Philips Ultrasound, LLC recalls Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232,…
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
Read the official notice →- Date
- 2026-01-07
- Country
- United States
- Brand
- Philips Ultrasound
- Product
- Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232,…
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of AK, AL, AR, AZ, CA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ultrasound recalls
- 2026-09-30
USPhilips Ultrasound, LLC recalls Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
Due to software issue with ultrasound system, doppler sample is displayed shallower than its actual measurement location, potentially causing inaccurate blood flow velocity measurements and misdiagnosis.
FDA · DevicePhilips Ultrasound, LLCWorldwide - US Nationwide distribution in the states of AL, CA, CT, FL, GA,…Official notice →- 2026-04-01
- US
Philips Ultrasound, Inc recalls Philips S5-2 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2025-12-10
- US
Philips Ultrasound, LLC recalls Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,
Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
FDA · DevicePhilips Ultrasound, LLCWorldwide US Nationwide distribution including in the states of AL, AR, AZ,…Official notice → - 2025-09-03
- US
Philips Ultrasound, Inc recalls TRANSDUCER L12-5 Transducer Probe
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2025-07-09
- US
Philips Ultrasound, Inc recalls Philips eL18-4 EMT Transducer.
Ultrasound transducer devices were refurbished beyond their useful life.
FDA · DevicePhilips Ultrasound, IncDomestic: Nationwide Distribution; Foreign: Australia, Austria, Belgium,…Official notice → - 2024-05-15
- US
Philips Ultrasound, Inc. recalls 5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/795143, 5500 W/795144, 5500 G/795145, and Product/REF: 5300…
Ultrasound system with: 1) transesophageal echocardiography transducer (TEE) connected/not selected 2) 1, 2 non-TEE connected 3) Imaging with non-TEE 4) Selected/not selected imaging transducer removed 5) Transducer…
FDA · DevicePhilips Ultrasound, Inc.Worldwide - US Nationwide distribution including in the states of CA, CO, CT,…Official notice →
Other drugs & medical recalls in the United States
- 2026-01-14
- US
Imprimis NJOF, LLC recalls Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL, Moxifloxacin 0.6 mg/ 0.6 mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46…
Presence of particulate matter - Glass like particles.
- US
Alembic Pharmaceuticals Limited recalls Fesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, Manufactured by: Alembic Pharmaceuticals Limited,…
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
- 2026-01-07
- US
Beaver-Visitec International, Inc. recalls BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not installed as intended. The omission of the ferrites on the USB…
FDA · DeviceBeaver-Visitec International, Inc.US Nationwide distribution in the states of FL, MI, OK, TX, WI.Official notice → - US
Sheathing Technologies Inc recalls Sheathes3D Seamless Viral Barrier, Latex-Free, 7/8"D Tapered to 2.9"W x 11.8"L (2.2cm Tapered to 7.4cm x 30cm), Non-Sterile,…
Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.
FDA · DeviceSheathing Technologies IncUS Nationwide distribution in the state of WA.Official notice → - US
Ferndale Laboratories, Inc. recalls Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number: 0523-48 Product Description: Liquid…
Butyrate tube cracks during actuation, rendering product unusable.
FDA · DeviceFerndale Laboratories, Inc.Worldwide distribution - US Nationwide and the country of UK.Official notice → - US
Vortex Surgical Inc. recalls Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.