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Class 2 Device Recall RUSCH ENDOBRONCHIAL TUBE SETS |
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Date Initiated by Firm |
November 21, 2014 |
Date Posted |
August 18, 2015 |
Recall Status1 |
Terminated 3 on August 15, 2017 |
Recall Number |
Z-2412-2015 |
Recall Event ID |
71727 |
510(K)Number |
K951091
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Product Classification |
Tube, bronchial (w/wo connector) - Product Code BTS
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Product |
Tracheopart Set (Left), Sterile |
Code Information |
Produce Code 116400-000750 Batch Number 13FT06, 13GE28J, 13GE31J, 13GT11, 13GT29, 13IT05, 13IT16, 13JT11, 13JT21R, 13JT25R, 13KT05R, 13LT11, 14BT09, 14BT15, 14CT16, 14CT20, 14DE16J, 14DT19, 14FE24J, 14FT16, 14GE29J, 14GT03, 14GT23, 14HT03, 14HT23, 14IT05, 14IT17; Product Code 116400-000850 Batch Number 13FT18, 13GE31J, 13GT05, 13HT17, 13IT13, 13JT15, 13JT20, 13JT20R, 13KT23R, 13LT08, 14BT09, 14BT15, 14CT16, 14CT20, 14DE15J, 14DT08, 14FE24J, 14FT13, 14GE28J, 14GT18, 14GT21, 14HT09, 14IT05, 14IT14, 14JT04, 14JT12; Product Code 116400-000950 Batch Number 13GE30J, 13GT29, 13HT16, 13IT13, 13LT08, 14AE05J, 14DT10, 14ET11, 14FT04, 14GT21, 14IT08, 14IT14, 14JE43J, 14JT18, 14JT24 |
Recalling Firm/ Manufacturer |
Teleflex, Inc. 550 E Swedesford Rd Ste 400 Wayne PA 19087-1601
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For Additional Information Contact |
610-378-0131
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Manufacturer Reason for Recall |
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
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FDA Determined Cause 2 |
Other |
Action |
Recall letters were sent on 11/21/2014 to consignees requesting them to discontinue use and quarantine the products. The letter includes a reply form to be returned. The letter to the distributors requested a sub-recall, and included a recall letter to be sent to their accounts. |
Distribution |
AL, AK, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MS, MO, NE, NV, NJ, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV. WI, DC, Puerto Rico, Canada, Bolivia, Ecuador, Hong Kong, Malaysia, Philippines, Taiwan, Trinidad & Tobago |
Total Product Life Cycle |
TPLC Device Report
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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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510(K) Database |
510(K)s with Product Code = BTS and Original Applicant = RUSCH INTL.
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