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U.S. Department of Health and Human Services

Class 2 Device Recall NovaGold

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 Class 2 Device Recall NovaGoldsee related information
Date Initiated by FirmMarch 31, 2014
Date PostedJune 10, 2014
Recall Status1 Terminated 3 on January 16, 2015
Recall NumberZ-1747-2014
Recall Event ID 68279
510(K)NumberK133076 
Product Classification Endoscopic guidewire, gastroenterology-urology - Product Code OCY
ProductBoston Scientific, NovaGold High Performance Guidewire, Rx only, Sterilized using ethylene oxide, UPN M00552010 and M00552000, Manufactured by NeoMetrics Inc, 2605 Fernbrook Lane Suite J, Plymouth, MN 55447. The NovaGold Guidewire is intended for use in selective cannulation of the biliary ducts including the common bile, pancreatic, cystic, right and left hepatic ducts, and to aid in the placement of diagnostic and therapeutic devices during endoscopic procedures.
Code Information MO26343, MO26345, MO26724, MO27402, MO26342, MO26344, MO26731, MO27401, MO27660, MO27901, MO27659, MO27820, MO27899 
Recalling Firm/
Manufacturer		 NEO METRICS, INC.
2605 Fernbrook Ln N Ste J
Plymouth MN 55447-4756
For Additional Information Contact
763-559-4440
Manufacturer Reason
for Recall		Neo Metrics, Inc. is recalling NovaGold Guidewire because the tip may uncoil and / detach more frequently than anticipated. There have been no reports of illness or injury.
FDA Determined
Cause 2		Nonconforming Material/Component
ActionNeoMetrics sent a letter dated March 31, 2014, to Boston Scientific. On March 24, 2014, Boston Scientific made NeoMetrics aware that Boston Scientific received 3 complaints from customers that the tip of the NovaGold guidewire detached and/or became uncoiled. Because the tips are breaking and/or uncoiling at a rate that was not anticipated, it has been decided that these units should be removed from the field. Therefore, NeoMetrics does not object to Boston Scientific executing this product removal in accordance with Section 4.4 of the distribution agreement. For further questions please call (763) 559-4440.
Quantity in Commerce1256 boxes ( 2 wires/box)
DistributionWorldwide Distribution - US and the countries of Austria, Belgium, Germany, Spain, France, Great Britain, Italy, Netherlands and Sweden.
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 = OCY
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