| Class 2 Device Recall BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010 | |
Date Initiated by Firm | March 07, 2019 |
Create Date | April 10, 2019 |
Recall Status1 |
Terminated 3 on May 12, 2020 |
Recall Number | Z-1122-2019 |
Recall Event ID |
82317 |
510(K)Number | K972404 |
Product Classification |
Tubes, vials, systems, serum separators, blood collection - Product Code JKA
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Product | BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010 |
Code Information |
Lot Numbers, UDI: 18041501, (17)210315(10)18041501, (01)50885403235915. 18042501, (17)210325(10)18042501, (01)50885403235915. 18050501, (17)210405(10)18050501, (01)50885403235915. 18051501, (17)210415(10)18051501, (01)50885403235915. 18052501, (17)210425(10)18052501, (01)50885403235915. 18060501, (17)210505(10)18060501, (01)50885403235915. 18061501, (17)210515(10)18061501, (01)50885403235915. 18062501, (17)210525(10)18062501, (01)50885403235915. 18070501, (17)210605(10)18070501, (01)50885403235915. 18072501, (17)210625(10)18072501, (01)50885403235915. 18080501, (17)210705(10)18080501, (01)50885403235915. 18081501, (17)210715(10)18081501, (01)50885403235915. |
Recalling Firm/ Manufacturer |
Becton Dickinson & Company 1 Becton Dr Franklin Lakes NJ 07417-1815
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For Additional Information Contact | 888-237-2762 |
Manufacturer Reason for Recall | The luer could break and cause the device to leak or break off and get stuck in the fistula needle port rendering the port inaccessible for dialysis. As a result, the patient would need to be re-cannulated with a new fistula needle to obtain their dialysis treatment. |
FDA Determined Cause 2 | Process change control |
Action | Urgent Medical Device Recall notification letters dated 3/7/19 were distributed to customers. |
Quantity in Commerce | 6,509,600 |
Distribution | US distribution to the states of FL and NJ. |
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 = JKA
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