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 2 Device Recall Bronchovideoscope BF1T180

  • 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 2 Device Recall Bronchovideoscope BF1T180see related information
Date Initiated by FirmAugust 08, 2018
Create DateSeptember 29, 2018
Recall Status1 Terminated 3 on May 17, 2022
Recall NumberZ-3285-2018
Recall Event ID 80925
510(K)NumberK061313 
Product Classification Bronchoscope (flexible or rigid) - Product Code EOQ
ProductBronchovideoscope BF-1T180
Code Information all lot codes
Recalling Firm/
Manufacturer		 Olympus Corporation of the Americas
3500 Corporate Pkwy
PO Box 610
Center Valley PA 18034-0610
For Additional Information ContactLaura Storms
484-896-5688
Manufacturer Reason
for Recall		The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
FDA Determined
Cause 2		Other
ActionUrgent Medical Device Safety Notice letters dated 8/8/18 were distributed to customers. The letters instructed customers to perform the following: Our records indicate that your facility has purchased one or more of the above-referenced endoscopes. OLYMPUS requires that you take the following actions: Inspect your inventory for the referenced Olympus models. Please keep this customer letter in your inventory and conduct the following action prior to every use. Step 1: Wearing sterile gloves, attempt to rotate or turn the instrument channel port in counter-clock direction as shown in picture 01. If the instrument channel port is able to be rotated or turned, do not use the endoscope and return it to Olympus for repair. If the instrument channel port does not rotate or turn, go to step 2. Step 2: Visually inspect the rubber part around the instrument channel port of the referenced endoscope. If the rubber part is in a normal condition as shown in picture 02, the endoscope can be used in a patient procedure. If the rubber part is lifted from the molding parts as shown in picture 03, do not use the endoscope and return it to Olympus for repair. If you have any questions about how to conduct this important inspection or you are not sure of the results of your inspection, you should contact the Olympus Technical Assistance Center (TAC), prior to using the device again. The phone number for TAC is 1-800-848-9024 option 1. To request service for your endoscope, contact Olympus at 1-800-848-9024, option 3. If you may have further distributed this product, please identify your customers and inform them at once of this action. Please complete and return the enclosed Reply Form to Olympus at facsimile (484) 896-7128.
Quantity in Commerce5810
DistributionThe products were distributed US nationwide and Canada.
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.
510(K) Database510(K)s with Product Code = EOQ
-
-