Midland Deluxe Mat Platform- Model C2237A, B and C
FDA Recall Z-1208-06 · Posted 2006-07-12
Recalling FirmSAMMONS PRESTON ROLYAN
Recall StatusTerminated
Product CodeINT
Date Initiated2006-01-25
Date Terminated2007-04-01
Product Quantity8 devices total
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.
Firm Action
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
Distribution Pattern
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, VA, VT, WA, WI, WV.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.