FDAClass IIJune 12, 2013

Hand Controls for Operon D750 recall

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

Why was Hand Controls for Operon D750 recalled?

The firm received complaints for unintended movements.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

The hand controls are neither serialized nor lot coded.

Product
Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables
Recalling firm
Berchtold Corp.
Quantity
3763
Distribution
Nationwide Distribution
Recall date
June 12, 2013
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls