ClearanceBrief
Recall Z-2834-2011 ยท EAZ Light, Operating, Dental

Dental Equipment LLC

LuxStar Dental Light have the following Agency model or Catalog Model numbers as ML1000, OL1000, CL1000, WL1000, CB1000, TL1000, and UL1000. The product is labeled in part: " Marus Dental***Mfg By: Dental Equipment LLC.***705 S. Springbrook Rd Building C Newberg, Oregon, 97132 USA***Dental Light***MN ML1000***". Product Usage: The intended use of the dental light is used for illuminating the or

DateJul 15, 2011 (initiated May 27, 2011)
StatusTerminated
ReasonLens heat shield (birdcage) of the Luxstar Dental Light could fall and injure a patient.
Root causeDevice Design
ActionDental Equipment, LLC sent an "URGENT MEDICAL DEVICE RECALL" notification letter via USPS 1st class to US consignees and via Federal Express or Fax to foreign consignees on June 24, 2011. The letter informed customers about the product, problem and tether upgrade corrective action. A Field Correction Acknowledgement Form and the Field Correction Completion Form was attached for customers to complete and return via the fax number 503-537-3617. The letter states that customers are to review their records in order to identify where the affected devices are located and which are still in service
Quantity13,226 units distributed worldwide
DistributionWorldwide Distribution -- USA (nationwide) including states of: CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, and Puerto Rico and the countries of: Australia, Belgium, Canada, France, Ge
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.