FDA Enforcement Class II Terminated

DX-D600 - DXD Imaging Package

Recall: Z-1738-2017 · Reported April 12, 2017

Enforcement

Recall Number
Z-1738-2017
Event ID
76840
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
AGFA Healthcare Corp.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
April 12, 2017
Initiation Date
May 2, 2016
Classification Date
April 5, 2017
Termination Date
April 10, 2017
Address
10 S Academy St, N/A, Greenville, SC, 29601-2632, United States

Description

DX-D600 - DXD Imaging Package

Reason

One of the dent markers from the DX-D600 dropped down from the overhead rail.

Code Info

A5430000264, A5430000272, A5430000162, A5430000238, A5430000226, A5430000137, A5430000306, A6430000298, A5430000299, A5430000246, A5430000247, A5430000249, A5430000303, A5430000228, A5430000229, A5430000304, A5430000234, A5430000276, A5430000285, A5430000296, A5430000300, A5430000015, A5430000124, A5430000125, A5430000095, A5430000144, A5430000156, A5430000206, A5430000207, A5430000061, A5430000100, A5430000053, A5430000079, A5430000225, A5430000248, A5430000027, A5430000030, A5430000042, A5430000052, A5430000066, A5430000068, A5430000081, A5430000085, A5430000096, A5430000131, A5430000132, A5430000224, A5430000297, A5430000166, A5430000222, A5430000054, A5430000263, A5430000057, A5430000119, A5430000133, A5430000176, A5430000177, A5430000184, A5430000295, A5430000275, A5430000279, A5430000107, A5430000108, A5430000293, A5430000063, A5430000020, A5430000074, A5430000045, A5430000121, A5430000089, A5430000143, A5430000218, A5430000199, A5430000149, A5430000060, A5430000165, A5430000067, A5430000130, A5430000305, A5430000215, A5430000237, A5430000058, A5430000105, A5430000106, A5430000172, A5430000183, A5430000242, A5430000281

Distribution

AL, CA, DC, FL, GA, HI, IL, IN, KS, LA, MA, MN, MO, NV, NJ, NM, NY, OH, OK, OR, SC, TN, TX, VA, and Canada

Quantity

81 units