Z-2288-2010

ReliaMed Deluxe Portable Adjusting Table. Product is a medical table used on patients for massage and...

Name: Z-2288-2010 ReliaMed Deluxe Portable Adjusting Table. Product is a medical table used on patients for massage and...
Creator: MDC Acquisition Co.
Published: 2010-04-23
License: https://open.fda.gov/license/

MDC Acquisition Co. / initiated 2010-04-23 / Terminated / root cause: design

FDA source

MDC Acquisition Co. began a recall of ReliaMed Deluxe Portable Adjusting Table. Product is a medical table used on patients for massage and chiropractic treatment on 2010-04-23. The reason FDA records is "Two complaints were received of the vinyl-covered, padded, plywood table surface breaking near the foot end". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-2288-2010
Status: Terminated
Initiated: 2010-04-23
Posted: 2010-08-26
Terminated: 2012-02-16
Recalling firm: MDC Acquisition Co.
Product: ReliaMed Deluxe Portable Adjusting Table. Product is a medical table used on patients for massage and chiropractic treatment.
Product code: FPS Board, Bed
Reason for recall: Two complaints were received of the vinyl-covered, padded, plywood table surface breaking near the foot end.
Root cause tag: design
FDA root cause: Component design/selection
Action: "Urgent: Medical Device Recall" letters were sent to consignees from Milliken Medical and Meyer Distributing Company in April 2010 describing the issue. They instructed their customers to immediately stop use of the table. customers were instructed to return the tables to the firm with an enclosed Recall Form for future replacement, or for replacement with a comparable table from another menufacturer at no cost, or for refund of the original cost of the device. Consignees may contact Meyer Distributing Company at 800-472-4221 and Milliken Medical at 800-532-1356.
Quantity in commerce: 265 Tables
Distribution: Worldwide distribution: USA, including the states of: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA and WI, and the country of Canada.
Product codes and lots: The table do not bear lot or serial numbers; however there are two device identification numbers representative of two different colors. ZZRNT100BL (blue) ZZRMT100BLK (black)

Product code FPS

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)