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Devices
Device Recall MAJOR LAP PACK
Model / Serial
Code:900404 Lots: 140915488 exp. 10/31/15 141216330 exp. 12/31/15 141216438 exp. 12/31/15 141216438 exp. 12/31/15 150116533 exp. 2/28/16 150116807 exp. 2/28/16 150116808 exp. 2/28/16 150116809 exp. 2/28/16 150116810 exp. 2/28/16 150116811 exp. 2/28/16 150217401 exp. 2/28/16 150217402 exp. 2/28/16 150217404 exp. 2/28/16 150217405 exp. 2/28/16 150217403 exp. 2/28/16 150217406 exp. 2/28/16 150217407 exp. 2/28/16 150217408 exp. 2/28/16 150217409 exp. 2/28/16 150317803 exp. 3/31/16 150317805 exp. 3/31/16 150317808 exp. 3/31/16 150317807 exp. 3/31/16 150317809 exp. 3/31/16 150317806 exp. 3/31/16 150418397 exp. 4/30/16 150418398 exp. 4/30/16 150418399 exp. 4/30/16 150418400 exp. 4/30/16 150418499 exp. 4/30/16 150418500 exp. 4/30/16 150418501 exp. 4/30/16 150418498 exp. 4/30/16 150519002 exp. 5/31/16 150519004 exp. 6/30/16 150519003 exp. 6/30/16 150519005 exp. 6/30/16 150619464 exp. 6/30/16 150619463 exp. 6/30/16 150619385 exp. 6/30/16 150619466 exp. 6/30/16
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Distributed Only in Puerto Rico.
Product Description
MAJOR LAP PACK 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 MAJOR LAP PACK
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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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