Atlas FDA

ValueLine Mat Platform Model C2230A,B,C; C922-30A, B,and C; C6904, C6903, C6902, C6901. All tables have the standard pla

FDA device recall Z-1207-06 · posted 2006-07-12 · Terminated

Recall details

Recalling firm
SAMMONS PRESTON ROLYAN
Reason for recall
There have been reports of structural failure on the skirt of select tables. The risk to patients presented by possible structural failure of the skirt of the table is a slow collapse of the plinth which could cause the patient to be displaced.
Action taken
Letters were sent to customers certified mail on 1/25-26/2006 instructing them to take the tables out of service until it could be inspected by a sales representative. Sales represenatives are following up with customers in person to inspect tables.
Root cause
Other
Status
Terminated
Product code
INT
Quantity affected
561 devices total
Distribution
Nationwide including the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, V
Date initiated
2006-01-25
Date posted
2006-07-12
Date terminated
2007-04-01
Location
Cedarburg, WI

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