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Recall Observatory FDA recall evidence

Device product

MyRay RXDC dental unit x-ray unit

Z-1217-2013

August 10, 2012

Class II

Product summary

Firm
CEFLA DENTAL GROUP
Event
Event 65036
Status
Terminated
Classification
Class II
Quantity
173 shipped to US
Official record key
device-enforcement:Z-1217-2013

Official wording

Reason: The RX DC dental x-ray unit was found to be noncompliant with 21CFR 1010,2, 1020.30(e) & 1020.30(h). Specifically, 1. The tube housing did not contain a Certification label. 2. The collimator did not contain an identification label. 3. The user's manual did not contain leakage technique factors, tube housing cooling curves and rating charts, and technique factors which lead to operation at ma

Code information: Model - MyRay RX DC

Distribution pattern: FOREIGN: CANADA; DOMESTIC: GA, TX, IL, CA, FL, NY, MA, AL, NJ, SC, WA, LA, MD, WY, CT, NM, WI, CO, NC, VA, PA and MI.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The RX DC dental x-ray unit was found to be noncompliant with 21CFR 1010,2, 1020.30(e) & 1020.30(h). Specifically, 1. The tube housing did not contain a Certification label. 2. The collimator did not contain an identification label. 3. The user's manual did not contain leakage technique factors, tube housing cooling curves and rating charts, and technique factors which lead to operation at ma