Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 3 Device Recall 20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
 Class 3 Device Recall 20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lenssee related information
Date Initiated by FirmOctober 25, 2012
Date PostedMarch 18, 2013
Recall Status1 Terminated 3 on June 11, 2013
Recall NumberZ-0966-2013
Recall Event ID 64410
Product Classification Lens, condensing, diagnostic - Product Code HJL
Product20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens For visualization during diagnosis and laser therapy of the human retina (fundus) using a binocular indirect ophthalmoscope.
Code Information Product Code: V20LC; Lot/Serial Numbers: BB09213 & BB09205 
Recalling Firm/
Manufacturer		 Volk Optical Inc
7893 Enterprise Dr
Mentor OH 44060-5309
For Additional Information ContactJacob Iselin
440-942-6161
Manufacturer Reason
for Recall		The defect was with mis-engraving of the lot # directly on the product and its packaging. Mixed up device engraving of V20LC (lot # BB09213) with that from V60C (lot # BB09205).
FDA Determined
Cause 2		Employee error
ActionVolk sent a Voluntary Medical Device Field Correction letter dated October 25, 2012, to all affected customers. The letter identifed the product, the problem, and the action to be taken by the customer. Customers were asked to correct their records with the correct lot number and to notify their customers of the voluntary field correction and request their compliance in updating their records. For questions customers were instructed to call 440-510-0800 or 440-942-6161. For questions regarding this recall call 440-942-6161.
Quantity in Commerce40 devices
DistributionWorldwide Distribution - USA including the states of AZ, CA, GA, MN, NJ, and NM. Internationally to Japan.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
-
-