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Device Recall LAPAROSCOPY PK
Model / Serial
Code:900474 Lots: 140915490 exp. 10/31/15 141216343 exp. 10/31/15 150116538 exp. 1/31/16 150116538 exp. 1/31/16 150317990 exp. 4/30/16 150317991 exp. 4/30/16 150518816 exp. 4/30/16 150619284 exp. 4/30/16 150619372 exp. 6/30/16
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
Distributed Only in Puerto Rico.
Product Description
LAPAROSCOPY PK 4/CS || Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. || .
Manufacturer
Customed, Inc
1 Event
Recall of Device Recall LAPAROSCOPY PK
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Manufacturer
Customed, Inc
Manufacturer Address
Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
Manufacturer Parent Company (2017)
Customed Inc
Source
USFDA
Language
English
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