Elekta, Inc. recalls MOSAIQ Oncology Information System
A drug strength in MOSAIQ can be changed during the ordering process and approved, but the saved drug strength reverts to the original value.
Read the official notice →- Date
- 2021-10-06
- Country
- United States
- Brand
- Elekta
- Product
- MOSAIQ Oncology Information System
- Classification
- Class II
- Units
- Distribution was made to CA, CO, FL, ID, LA, MO, MS, NC, NH, NM, NV, NY, OH,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Elekta recalls
- 2023-06-07
USElekta, Inc. recalls Elekta Medical Linear Accelerator (ELMA) included in the below platforms: a. Elekta Infinity; b. Versa HD; c. Elekta Synergy
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Re-optimization, after adding contours without forced density outside the external structure, may result in inaccurate dose presentation.
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A reconstruction error may occur when using the Catheter Bending functionality in Applicator Modeling or Implant Modeling
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Under certain circumstances, there can be a difference between the planned and delivered dose of the two ovoid channels.
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Elekta Inc recalls Elekta Monaco - Product Usage: used to make treatment plans for patients with prescriptions for external beam radiation therapy.
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Other drugs & medical recalls in the United States
- 2021-10-06
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