FDAFDA · Food and drugs·Recall number Z-1488-2013
Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables
Published June 12, 2013 · Recall initiated: March 12, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The firm received complaints for unintended movements.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Berchtold Corp.
- Distributor
- Nationwide Distribution
- Lot
- The hand controls are neither serialized nor lot coded.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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