Z-1209-06

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

Name: Z-1209-06 Midland Deluxe Mat Platform with Adjustable Backrest Model C5522-30A, B, and C
Creator: Sammons Preston Rolyan
Published: 2006-01-25
License: https://open.fda.gov/license/

Performance Health Supply / initiated 2006-01-25 / Terminated

FDA source

SAMMONS PRESTON ROLYAN began a recall of Midland Deluxe Mat Platform with Adjustable Backrest Model C5522-30A, B, and C on 2006-01-25. The reason FDA records is "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...". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1209-06
Status: Terminated
Initiated: 2006-01-25
Posted: 2006-07-12
Terminated: 2007-04-01
Recalling firm: Performance Health Supply
Product: Midland Deluxe Mat Platform with Adjustable Backrest Model C5522-30A, B, and C,
Product code: INT Plinth
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.
FDA root cause: Other
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.
Quantity in commerce: 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, VA, VT, WA, WI, WV.
Product codes and lots: Serial number prefixess 2509 throuth 2511

Product code INT

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)