Berchtold Corp.: Medical Device Recall in 2013 - (Recall #: Z-1488-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables

Product Classification:

Class II

Date Initiated: March 12, 2013

Date Posted: June 12, 2013

Recall Number: Z-1488-2013

Event ID: 65062

Reason for Recall:

The firm received complaints for unintended movements.

Status: Terminated

Product Quantity: 3763

Code Information:

The hand controls are neither serialized nor lot coded.

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated