Siemens Medical Solutions USA, Inc recalls YSIO X.Pree
For the automated multi-image-acquisition procedure Ortho x-ray collimation is set in a preparative stage for the entire examination area prior to the exam. During acquisition of each individual x-ray image, the x-ray…
Read the official notice →- Date
- 2022-04-13
- Country
- United States
- Brand
- Siemens Medical Solutions
- Product
- YSIO X.Pree
- Classification
- Class II
- Units
- US Nationwide, Worldwide distribution
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
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- 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 Siemens Medical Solutions recalls
- 2022-04-27
USSiemens Medical Solutions USA, Inc recalls Artis zee floor MN, Model Number 10094142
If the coolant level in the cooling circuit drops below a certain level, this may result in a situation in which the X-ray tube is no longer sufficiently cooled and the system will display the message "TUBE HOT, have a…
- US
Siemens Medical Solutions USA, Inc recalls SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now 11061610 & 11061618 SOMATOM go.Up 11061620 & 11061628…
Software error may result in sporadic problems causing scanning workflow interruptions, unexpected user notifications and image artifacts. Sporadic software errors may also occur during interventional workflows.…
- 2022-04-13
- US
Siemens Medical Solutions USA, Inc. recalls Symbia Intevo Bold and Symbia Intevo 6 SPECT/CT Systems
There is a quality issue with the three bolts that hold the CT balancing weights, which could create a safety issue.
FDA · DeviceSiemens Medical Solutions USA, Inc.Distribution OUS only to El Salvador, France, Germany, Japan, Taiwan, and UK.Official notice → - 2022-04-06
- US
Siemens Medical Solutions USA, Inc recalls Ysiosystem with VC10 software version, Model Number 10281013. Radiographic system
Siemens Healthineers has identified a software error in previous software version VB10 for the Ysio fully automated system. The unit may process incorrect internal values for the position of its ceiling tube stand. If…
- 2022-03-23
- US
Siemens Medical Solutions USA, Inc. recalls Diagnostic Ultrasound System, ACUSON Juniper, UDI: (01)04056869152059, Model: 11335791, Rx, CE Ultrasound imaging system…
The clip store function in the ultrasound imaging system does not work when the system has a disk full error. This could cause a delay in treatment if the ultrasound system is unable to save clips as study…
FDA · DeviceSiemens Medical Solutions USA, Inc.Worldwide distribution: US (nationwide) and countries of: Algeria, Andorra,…Official notice → - 2022-02-09
- US
Siemens Medical Solutions USA, Inc. recalls ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B
Due to a calculation error in the measurement when using 2D trace (manual trace) tool. The trace circumference value is overestimated and may potentially result in misdiagnosis of a patient's condition.
FDA · DeviceSiemens Medical Solutions USA, Inc.Worldwide distribution - U.S. Nationwide distribution in the states of AL, AK,…Official notice →
Other drugs & medical recalls in the United States
- 2022-04-13
- US
SA3, LLC recalls Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm
Due to failure of microbial testing for total aerobic microbial count (TAMC).
- US
GE Healthcare, LLC recalls Revolution Apex, Revolution CT with Apex Edition
The accumulated dose is incorrectly displayed in certain situations. There are two situations that will result in the SmartStep displayed dose being inaccurately high.
- US
Philips Healthcare recalls Philips StentBoost Live R2.0 application, when used with the Philips Azurion with software release R2.x
Due to an incorrect configuration setting in the EPX database of StentBoost Live, acquisition does not stop automatically as it should. When the user selects the StentBoost Live protocol on the Philips Azurion system,…
- US
SUN PHARMACEUTICAL INDUSTRIES INC recalls Cequa (cyclosporine ophthalmic solution) 0.09%, packaged in 6 pouches x 10 single-use vials (0.25 mL each) per box,…
Subpotent Drug and Presence of Particulate Matter: low out-of-specification results obtained for assay and the presence of particulate matter.
- US
Adamis Pharmaceuticals Corporation recalls SYMJEPI (epinephrine injection, USP) 0.15 mg (0.15 mg/0.3 mL), Two Pre-Filled Single-Dose Syringes per carton, Rx Only,…
Defective Delivery System: Potential clogging of the needle preventing the dispensing of epinephrine.
- US
Macleods Pharma Usa Inc recalls Risedronate Sodium Tablets, USP, 5 mg, Rx Only, 30-count bottle, Manufactured for: Macleods Pharma USA, Plainsboro, NJ 08536,…
FAILED CONTENT UNIFORMITY SPECIFICATIONS