Z-0182-04

Ronci Surgical Universal Imaging Extension used with the Ronci Pain Management Table System Catalog Number...

Name: Z-0182-04 Ronci Surgical Universal Imaging Extension used with the Ronci Pain Management Table System Catalog Number...
Creator: The OR Group
Published: 2003-11-06
License: https://open.fda.gov/license/

Allen Medical Systems, Inc. / initiated 2003-11-06 / Terminated

FDA source

The OR Group began a recall of Ronci Surgical Universal Imaging Extension used with the Ronci Pain Management Table System Catalog Number: R-934-25A on 2003-11-06. The reason FDA records is "Imaging table with extension may fail if the table leg is incorrectly positioned and the load exceeds the maximum weight of 400 lb". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0182-04
Status: Terminated
Initiated: 2003-11-06
Posted: 2003-12-10
Terminated: 2005-07-25
Recalling firm: Allen Medical Systems, Inc.
Product: Ronci Surgical Universal Imaging Extension used with the Ronci Pain Management Table System Catalog Number: R-934-25A
Product code: FPS Board, Bed
Reason for recall: Imaging table with extension may fail if the table leg is incorrectly positioned and the load exceeds the maximum weight of 400 lb
FDA root cause: Other
Action: The OR Group forwarded by 2nd day mail on 11/6/03 the repair kit and instructions to the accounts.
Quantity in commerce: 17 units
Distribution: Nationwide. CA, FL, GA, IA MI, MT, NH, OH, NJ, NY, SC, UT, TX, VA
Product codes and lots: S/N''S: R00043, R001080, R001092, R001198, R0001341, R001370, R001374, R001366, R001337, R001497, R001478, R001493, R001501, R001529, R001812, R001816, R002023.

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)