PTW FREIBURG recalls Brand Name: VERIQA; Product Name: RT MonteCarlo 3D v3; Model/Catalog Number: S070031.520; Software Version: 3.1.18;
When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead users to incorrectly omit the bolus during treatment…
Read the official notice →- Date
- 2026-09-23
- Country
- United States
- Brand
- Ptw-Freiburg
- Product
- Brand Name: VERIQA; Product Name: RT MonteCarlo 3D v3; Model/Catalog Number: S070031.520; Software Version: 3.1.18;
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of GA, NY and the…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ptw-Freiburg recalls
- 2024-02-28
USPTW-FREIBURG recalls Software VERIQA (S070031), version 2.0 and 2.1- Software package for display, evaluation and digital processing of medical image data sets…
Software: If the user excludes voxels from the Gamma calculation that are below a dose threshold (Suppress gamma calculation), the Gamma Passing Rate (GPR) calculated for individual ROIs is not correct. The GPR…
- 2023-09-20
- US
PTW-FREIBURG recalls BeamAdjust software Version 2.3.3 Ref: S080032 The following devices are affected when a relative calibration is performed using ArrayCal…
Generated calibration file will not be correct in case of a relative calibration of an OCTAVIUS Detector 1000 or OCTAVIUS Detector 1600, if a Tiff file or a DICOM data set is used as reference matrix. Therefore, the…
Other drugs & medical recalls in the United States
- 2026-09-23
- US
restor3d Inc. recalls Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide), REF: 5831-9006
Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fixation or poor alignment of implants,…
- US
Wilson-Cook Medical Inc. recalls Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7, HEMO-10, HEMO-7-EU,…
Due to issue with endoscope adherence and inability to spray powder. Firm will provide an updated Instruction for Use (IFU).
FDA · DeviceWilson-Cook Medical Inc.Worldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice → - US
Happiest Baby, Inc recalls Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101 S2107-110
Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA.
FDA · DeviceHappiest Baby, IncUS Nationwide distribution including in the states of Alabama, Alaska,…Official notice → - US
Straumann USA LLC recalls GM Helix Implant, REF: 109.984;
There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.
FDA · DeviceStraumann USA LLCUS Nationwide distribution in the states of AL, AZ, CA, CO, FL, GA, IL, KS,…Official notice → - US
WELL LEAD MEDICAL CO. LTD recalls SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25
The 6Fr suction catheter could not pass through the samples smoothly.
FDA · DeviceWELL LEAD MEDICAL CO. LTDUS Nationwide distribution in the state of MI.Official notice → - US
GE Healthcare recalls Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient…