Recall Z-2480-2014— Customed, Inc

Class I FDA medical device recall by Customed, Inc, initiated 2014-05-20, terminated 2017-08-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Extremity Pack, code 900-2615, contains: (5) LAP SPONGE PREWASH 18" X 18" XRD (1) ELASTIC BANDAGE WITH VELCRO 4 X 5 (2) BLADE SURGICAL# 15 STAINLES STEEL (4) DRAPE UTILITY WITH TAPE (1) GOWN XL SMS IMPERVIOUS REINFORCED ( 1) GOWN SURG REINFORCED LARGE TOWEL & WRAP (1) SKIN MARKER WITH RULER (1) TUBE SUCTION CONNECT Y4" X 12' ( 1) CAST PADDING SOFT ROLL 4" X 4yds (10) GAUZE SPONGE 4" X 4" 16PLY ( 1) MERLING SKIN PREP APPLIC 39ML (1) MAYO STAND COVER REINFORCED ( 1) TABLE COVER REINFORCED 50" X 90" (2) DRAPE SHEET 42" X 55" ( 1) STOCKINETTE 9" x 48" (1) CAUTERY PENCIL ROCKER SWITCH (2) LITE GLOVE ( 1) BANDAGE ESMARK 6" X 9yds ( 1) SHEET EXTREMITY ABS SMS 125" X 85" ( 1) UTILITY BOWL QUART 32oz Product Usage: EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.. Reason: Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition..

Recalling firm

Customed, Inc

Classification

Class I

Status

Terminated

Initiated

2014-05-20

Terminated

2017-08-14

Firm location

Fajardo, PR, United States

Data sourced from openFDA. This site is unofficial and independent of the FDA.