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 BK Medical

  • 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 BK Medical see related information
Date Initiated by Firm January 24, 2008
Date Posted June 10, 2008
Recall Status1 Terminated 3 on June 23, 2008
Recall Number Z-1140-2008
Recall Event ID 46394
510(K)Number K024236  K043524  
Product Classification ultrasound transducer - Product Code IYN
Product B-K Medical Intraoperative Transducer Type 8814, diagnostic ultrasound transducer, B-K Medical Systems, Inc., Wilmington, MA 01887
Code Information Serial Numbers: 1864742, 1869148, 1869619, 1870824, 1870825, 1872061, and 1875317.  
Recalling Firm/
Manufacturer		 B & K Medical Systems, Inc.
250 Andover St
Wilmington MA 01887-1048
For Additional Information Contact SAME
800-876-7226
Manufacturer Reason
for Recall		 Crack: Incomplete glue joint in the device housing may affect electrical safety or sterilization.
FDA Determined
Cause 2		 Process control
Action B-K Medical issued letter notification on 1/23/08 to accounts via Fed Ex, advising them not to use the unit until a representative can inspect and exchange, if unit is found defective. Instructions are also provided to continue use of the device with a sterile cover until site visit.
Quantity in Commerce 7
Distribution USA Distribution: MA, MI, PA, TX, and OR.
Total Product Life Cycle TPLC 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) Database 510(K)s with Product Code = IYN and Original Applicant = B-K MEDICAL A/S
-
-