FDA Recall Terminated

Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals to illuminate the oral cavity while performing examinations and dental procedures.

Recall: Z-1268-2016 · Initiated March 8, 2016

Recall

Recall Number
Z-1268-2016
Event Number
73460
Firm
Pelton & Crane Marus DCI Equipment KaVo
FEI Number
1017522
Product Code
EAZ
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
March 8, 2016
Terminated
June 6, 2016
Address
11727 Fruehauf Dr, Charlotte, NC, 28273-6507

Description

Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals to illuminate the oral cavity while performing examinations and dental procedures.

Reason

The firm received two customer complaints local Pelton & Crane distributors that the Helios 3000 track mounted dental lights were missing the two 8/32x3/16 set screws during the initial installation of the dental light.

Action

Pelton & Crane sent an Urgent Medical Device Recall letters to affected customers on March 8, 2016 and will be completed by 3/11/2016. The letter identified the affected product, problem and actions to be taken. Customers were instructed to complete and return the Field Correction Acknowledgement Form in the enclosed self-address stamped envelope to Pelton & Crane. For questions or concerns regarding this recall please call 1-800-659-6560, ext. 7227.

Distribution

US Nationwide Distribution in the states of AZ, AR, CA, CO, CT, FL, IA, ID, IL, IN, MA, MI, MN, NJ, NY, NC, OH, OR, PA, TN, TX, UT, VA, WI and Canada

Quantity

156 units