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U.S. Department of Health and Human Services

Class 1 Device Recall Hudson RCI Sheridan EZENDO

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  Class 1 Device Recall Hudson RCI Sheridan EZENDO see related information
Date Initiated by Firm May 24, 2019
Create Date June 19, 2019
Recall Status1 Open3, Classified
Recall Number Z-1761-2019
Recall Event ID 82964
510(K)Number K822082  
Product Classification Tube, tracheal (w/wo connector) - Product Code BTR
Product Hudson RCI Sheridan:
1) EZ-ENDO 6.0 mm, Product Code 5-22512
2) EZ-ENDO 6.5 mm, Product Code 5-22513
3) EZ-ENDO 7.0 mm, Product Code 5-22514
4) EZ-ENDO 7.5 mm, Product Code 5-22515
5) EZ-ENDO 8.0 mm, Product Code 5-22516
6) EZ-ENDO 8.5 mm, Product Code 5-22517

Product Usage:
Tracheal tube/airway management
Code Information 1) EZ-ENDO 6.0 mm, Product Code 5-22512 Lot Numbers: 73K1600152 73M1600163 73A1700280 73C1700567 73E1700496 73F1700403 73H1700347 73M1700272 73E1800401 73E1800575 73F1800354  2) EZ-ENDO 6.5 mm, Product Code 5-22513 Lot Numbers: 73J1600766 73B1700155 73C1700568 73F1700404 73G1700432 73H1700348 73E1800576 73F1800355  3) EZ-ENDO 7.0 mm, Product Code 5-22514 Lot Numbers: 73A1700118 73C1700569 73E1700722 73F1700175 73F1700405 73G1700433 73H1700349 73H1700494 73H1700711 73J1700143 73K1700081 73K1700610 73L1700181 73M1700273 73D1800653 73F1800562 73F1800720 73H1800450 73J1800531 73K1800328 73K1800786  4) EZ-ENDO 7.5 mm, Product Code 5-22515 Lot Numbers: 73B1700316 73C1700262 73C1700418 73E1700723 73E1700104 73F1700176 73F1700406 73G1700434 73H1700350 73J1700302 73J1700497 73K1700747 73M1700274 73A1800068 73A1800683 73B1800502 73C1800201 73D1800154 73E1800402 73F1800565 73G1800591 73H1800451 73H1800686 73J1800113 73K1800736  5) EZ-ENDO 8.0 mm, Product Code 5-22516 Lot Numbers: 73K1600594 73A1700282 73B1700158 73B1700317 73C1700570 73F1700036 73F1700177 73F1700407 73G1700614 73H1700495 73J1700487 73K1700082 73A1800684 73B1800503 73C1800371 73E1800577 73G1800232 73J1800532 73K1800327  6) EZ-ENDO 8.5 mm, Product Code 5-22517 Lot Numbers: 73J1600767 73C1800202   
Recalling Firm/
Manufacturer
Teleflex Medical
3015 Carrington Mill Blvd
Morrisville NC 27560-5437
Manufacturer Reason
for Recall
This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.
FDA Determined
Cause 2
Under Investigation by firm
Action Teleflex sent an Urgent Medical Device Recall letter dated May 24, 2019 to customers. The letter identified the affected product, problem and actions to be taken. The letter directed customers to discontinue use, quarantine the product, and contact Teleflex for return of the product. Distributors were directed to notify their customers and request the customer return the recalled products to them for consolidation and subsequent return to Teleflex.. For questions contact your local sales representative or Customer Service at 1-866-396-2111
Quantity in Commerce 55312 units
Distribution Worldwide - US Nationwide Distribution
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = BTR and Original Applicant = SHERIDAN CATHETER CORP.
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