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 Elutia Hubless Coated Silicone Wound Drain

  • 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 Elutia Hubless Coated Silicone Wound Drainsee related information
Date Initiated by FirmJanuary 28, 2013
Date PostedMarch 11, 2013
Recall Status1 Terminated 3 on July 08, 2013
Recall NumberZ-0936-2013
Recall Event ID 64326
510(K)NumberK063245 
Product Classification Drainage catheter with antibiotic - Product Code OEI
ProductBacterin Elutia, Hubless Coated Silicone Surgical Wound Drain 24 Fr Round Hubless, Full-Fluted Coated with Silver Sulfadiazine STERILE, Box of 10 Part #7118. Indicated for use in surgical wound drainage.
Code Information 005312; 011012; 012111; 012311; 012511; 013011; 019212; 023611; 023811; 024011; 024211; 025912; 033611; 042211
FEI Number 3005031160
Recalling Firm/
Manufacturer		 Bacterin International, Inc.
600 Cruiser Ln
Belgrade MT 59714-9719
For Additional Information ContactJanet Seidel
406-388-0480
Manufacturer Reason
for Recall		A portion of a silicone wound drain was found to be cracked.
FDA Determined
Cause 2		Nonconforming Material/Component
ActionConsignees were informed of the recall via e-mail beginning 1/28/13 with a request for a return response. This was followed by a "Voluntary Product Recall Information" letter dated 2/13/13 that described the product issue and provided recommended actions. The firm asked for all product to be returned to them.
Quantity in Commerce15 boxes (10/box) to 4 consignees in US and 81 boxes (10/box) to 1 foreign consignee
Distribution13 US consignees located in CA, CO, MT, TX, UT, and VA. This represents 4 customers and 9 other individual contacts in USA that received marketing samples. Plus 4 Bacterin representives nationwide received samples. Foreign Consingee
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 = OEI
-
-