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U.S. Department of Health and Human Services

Class 1 Device Recall HUDSON RCI

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  Class 1 Device Recall HUDSON RCI see related information
Date Initiated by Firm June 01, 2015
Date Posted August 20, 2015
Recall Status1 Terminated 3 on April 16, 2018
Recall Number Z-2369-2015
Recall Event ID 71360
Product Classification Tube, tracheal/bronchial, differential ventilation (w/wo connector) - Product Code CBI
Product HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile.

Used to aspirate liquids or semisolids from a patient's upper airway.
Code Information Product Code: 5-16142, Lot numbers: 01J1300535, 01M1300215, 01A1400321, 73D1400579 and 73E1400113.
Recalling Firm/
Manufacturer		 Teleflex Medical
2917 Weck Dr
Research Triangle Park NC 27709-0186
For Additional Information Contact Tara Torres
610-378-0131
Manufacturer Reason
for Recall		 The double swivel connector may crack or separate on the endobronchial tube.
FDA Determined
Cause 2		 Unknown/Undetermined by firm
Action Teleflex Medical sent an Urgent Medical Device Recall Notification letter dated June 1, 2015 to their customers. The letter identified the affected product, problem and actions to be taken. Customers were directed to contact any customers who had received the product included within the scope of this recall. Customers were directed to immediately discontinue use and quarantine any products with the referenced catalog numbers and lot numbers listed in the notification. Additionally, customers were asked to return any affected product together with a completed Recall Acknowledgement Form, for consolidation and return to Teleflex Medical. For questions contact your local sales representative or Customer Service at 1-866-246-6990.
Quantity in Commerce 188,195 total units
Distribution Worldwide Distribution - US (nationwide) and the countries of: The Bahamas, Belgium, Argentina, Canada, China, India, Japan, South Korea, Mexico, New Zealand and Vietnam.
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.
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