Operon Electrical Operating Room Table. The device is used as an electrical operating room table.
FDA device recall Z-1123-2009 · posted 2009-04-27 · Terminated
Recall details
- Recalling firm
- Berchtold Corp.
- 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.
- 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.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- GDC
- Quantity affected
- 453 units
- Distribution
- Worldwide Distribution -- US and Canada.
- Date initiated
- 2009-02-02
- Date posted
- 2009-04-27
- Date terminated
- 2009-06-04
- Location
- N Charleston, SC
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