Operon Electrical Operating Room Table. The device is used as an electrical operating room table.
This recall has been terminated (originally issued April 27, 2009).
- Company
- Berchtold Corp.
- Recall Initiated
- February 2, 2009
- Posted
- April 27, 2009
- Terminated
- June 4, 2009
- Recall Number
- Z-1123-2009
- Quantity
- 453 units
- Firm Location
- Charleston, SC
- Official Source
- View on FDA website ↗
Reason for Recall
Difficulty in pressing the button needed to release a bed part resulted in an injury to a caregiver's finger which became stuck in metal latch under the gas cylinder of the bed piece.
Distribution
Worldwide Distribution -- US and Canada.
Lot / Code Info
D 850, D750, D 752 and B 810.
Root Cause
Device Design
Action Taken
An official notification letter dated February 3, 2009 was hand-carried by a local Berchtold Corporation Technical Service representative to each account. The letter indicated that the Berchtold Corporation Service Technician will complete recommended upgrades. Direct questions concerning this recall to your BERCHTOLD Technician Service at 1-800-243-5135 and press the Number 2.
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