Midland Deluxe Mat Platform with Adjustable Backrest Model C5522-30A, B, and C,

FDA device recall Z-1209-06 · 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

831 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