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U.S. Department of Health and Human Services

Class 2 Device Recall Pinnacle Destination Guiding Sheath, 6 French, 90 cm

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 Class 2 Device Recall Pinnacle Destination Guiding Sheath, 6 French, 90 cmsee related information
Date Initiated by FirmJune 24, 2010
Date PostedJune 06, 2011
Recall Status1 Terminated 3 on July 07, 2011
Recall NumberZ-2415-2011
Recall Event ID 58677
510(K)NumberK012812 
Product Classification Introducer, catheter - Product Code DYB
ProductPinnacle Destination Guiding Sheath, 6 French, 90 cm, Straight Tip, Tuohy-Borst Valve, Lot MD24, MD31, ME07, & ME14. 510(k) K012812 Guiding Sheath is used to facilitate the introduction of interventional and diagnostic devices into the human vasculature, including but not limited to the renal arteries for the Renal Guiding Sheath and the carotid arteries for the Carotid Guiding Sheath.
Code Information RSC01
Recalling Firm/
Manufacturer		 Terumo Medical Corporation
950 Elkton Blvd
Elkton MD 21921-5322
For Additional Information ContactKathleen Little, PhD
410-392-7123
Manufacturer Reason
for Recall		Molding defect in destination product that render the device unusable.
FDA Determined
Cause 2		Equipment maintenance
ActionTerumo Medical Corporation sent an Urgent Product Bulletin Recall letter dated June 24, 2010, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Terumo requested customers to immediately discontinue use, and quarantine any available stock of the listed product codes. In order to facilitate the exchange of these devices, a Terumo Territory Manager contacted all customers by July 9th to confirm receipt of the Terumo Destination Bulletin and scheduled an appointment to visit each customer in person by July 31st to personally manage the exchange. For questions or for further information, call (800) 283-7866 and ask to speak with the Product Recall Coordinator.
Quantity in Commerce214 units
DistributionWorldwide Distribution - USA including AL, AK, AZ, TX, LA, MS, MN, MO, CA, GA, FL, HI, KS, IA, ID, IL, TN, NM, OR, OK, WA, and WI and the countries of Belgium, Brazil, and Panama
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 = DYB
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