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FDA Medical Device Recalls (openFDA)

Berchtold Corp.: Operon Electrical Operating Room Table. The device is used as an electrical operating room table.

Recall number
Z-1123-2009
Recalling firm
Berchtold Corp.
Product
Operon Electrical Operating Room Table. The device is used as an electrical operating room table.
Status
Terminated
Initiated
2009-02-02
Posted
2009-04-27
Terminated
2009-06-04
Reason
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.
Root cause
Device Design
Action
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.
Quantity
453 units
Distribution
Worldwide Distribution -- US and Canada.
Lot, serial or model codes
D 850, D750, D 752 and B 810.
510(k) numbers
not on file
PMA numbers
not on file
Product code
GDC
Firm FEI
1220685
Firm city
N Charleston
Firm state
SC
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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