ExacTrac Dynamic software model numbers: 20910-01, ETD Positioning and Moni. 1.0.0 INST; 20910-01A, ETD Positioning
Summary
The FDA issued a Class II for ExacTrac Dynamic software model numbers: 20910-01, ETD Positioning and Moni. by Brainlab AG. Reason: The yaw angle may be incorrect for CBCT positioning workflows using setup beams with Varian LINACs..
Details
Source
Device Recall
External ID
Z-0733-2022
Action Date
2022-03-16
Status
Ongoing
Category
device
Product Description
ExacTrac Dynamic software model numbers: 20910-01, ETD Positioning and Moni. 1.0.0 INST; 20910-01A, ETD Positioning and Moni. 1.0.1 INST; 20910-01B, ETD Positioning and Moni. 1.0.2 INST; and 20910-01C ETD Positioning and Moni. 1.0.3 INST.
Lot/Code Info: Software versions 1.0.0, 1.0.1, 1.0.2, 1.0.3, GTIN 04056481142315.
Quantity Affected: 205 systems
Reason for Recall
The yaw angle may be incorrect for CBCT positioning workflows using setup beams with Varian LINACs.
Distribution
Distribution was made to AZ, AR, CA, CO, FL, GA, IN, KY, MD, MS, MO, NJ, NY, NC, OK, OR, PA, TX, VA, and WA. There was no government or military distribution. Foreign distribution was made to Australia, Austria, Bahrain, Belgium, China, Denmark, France, Germany, Hong Kong, India, Ireland, Israel, Italy, Japan, Jordan, New Zealand, Poland, Singapore, Slovakia, South Korea, Spain, Thailand, Turkey, United Kingdom, and United Arab Emirates.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-25
Company
Munich, N/A
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 143 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Brainlab AG has 32 FDA actions in our database, including 4 recalls and 28 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Brainlab AG) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Brainlab AG have FDA actions?
Brainlab AG has 32 FDA actions in our database, including 4 recalls and 28 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0733-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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