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U.S. Department of Health and Human Services

Class 2 Device Recall Operon

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 Class 2 Device Recall Operonsee related information
Date Initiated by FirmFebruary 02, 2009
Date PostedApril 27, 2009
Recall Status1 Terminated 3 on June 04, 2009
Recall NumberZ-1123-2009
Recall Event ID 51276
Product Classification Electrical Operating-Room Table - Product Code GDC
ProductOperon Electrical Operating Room Table. The device is used as an electrical operating room table.
Code Information D 850, D750, D 752 and B 810.
FEI Number 1220685
Recalling Firm/
Manufacturer		 Berchtold Corp.
1950 Hanahan Rd
N Charleston SC 29406-4878
For Additional Information ContactHeath Hines
800-243-5135 Ext. 263
Manufacturer 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.
FDA Determined
Cause 2		Device Design
ActionAn 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.
Quantity in Commerce453 units
DistributionWorldwide Distribution -- US and Canada.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 �7.55.
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