Monaco RTP System Radiation treatment planning
Reported: October 2, 2013 Initiated: July 2, 2013 #Z-2276-2013
Product Description
Monaco RTP System Radiation treatment planning
Reason for Recall
Upgrade installation script is designed to overwrite the same pouch files in the Treatment Couch Library with the original default values.
Details
- Recalling Firm
- Elekta, Inc.
- Units Affected
- 45
- Distribution
- Nationwide Distribution including AK, CA, CO, CT, FL, IL, IN, MI, MN, MO, NC, NJ, NY, OH, OK, OR, PA, SC, TN, TX, WA and Puerto Rico.
- Location
- Atlanta, GA
Frequently Asked Questions
What product was recalled? ▼
Monaco RTP System Radiation treatment planning. Recalled by Elekta, Inc.. Units affected: 45.
Why was this product recalled? ▼
Upgrade installation script is designed to overwrite the same pouch files in the Treatment Couch Library with the original default values.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 2, 2013. Severity: Moderate. Recall number: Z-2276-2013.
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