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FDA Medical Device Recalls (openFDA)

Linet Spol. S.r.o.: Eleganza 5 (AC powered adjustable bed), Item Numbers: a) 1GE512055-40, b) 1GE512055-45, c) 1GE512055-85, and d) 1GE512055-95 - Product Usage: Eleganza 5 is a positionable bed for intensive care. Its purpose is to support patient and to facilitate treatment and manipulation with patient for nursing personnel.

Recall number
Z-0767-2021
Recalling firm
Linet Spol. S.r.o.
Product
Eleganza 5 (AC powered adjustable bed), Item Numbers: a) 1GE512055-40, b) 1GE512055-45, c) 1GE512055-85, and d) 1GE512055-95 - Product Usage: Eleganza 5 is a positionable bed for intensive care. Its purpose is to support patient and to facilitate treatment and manipulation with patient for nursing personnel.
Status
Open, Classified
Initiated
2019-11-13
Posted
not on file
Terminated
not on file
Reason
A component used within the side rail mechanism may malfunction, resulting in the side rail either not locking properly in the upper position or the side rail becoming stuck in the upper position.
Root cause
Device Design
Action
The firm initiated the recall by email and hand delivery on 11/13/2019. The notice explains the malfunction and risk, and provides the following information: "Advice on action to be taken by the user: Linet has developed a correction for the side rail mechanism. We will contact you to schedule a Linet or partner technician to update your affected Eleganza 5 Beds with this correction. Until your affected beds are updated, we ask that you follow the safety information as outlined in the Eleganza 5 User manual (D9U001GE5-0101, version: 11, Publication date: 2019-11 (available at your local distributor)) when operating the side rails. Section 11.1 Side rails Chapter MANIPULATION To raise siderails up: >Grab side rail by Side Rail Handle, >Pull side rail up until it latches. You will hear audible "click". If you raise the side rails to the upper position and you find the side rail is not secured and/or no audible click is heard during this operation, take the bed out of service until the bed has been updated." Contact Linet Technical Services at phone no.: 877-815-9897
Quantity
518 units
Distribution
US Nationwide distribution.
Lot, serial or model codes
a) 1GE512055-40: 20170042941, 20170042942, 20170042943, 20170042944, 20170042945, 20170042946, 20170043764, 20170043765, 20170043766, 20170043767, 20170043768, 20170043769, 20170043770, 20170043771, 20170043772, 20170043773, 20170043774, 20170043775  b) 1GE512055-45: 20170055478, 20170055479, 20170055480, 20170055481, 20170055482, 20170055483, 20170055484, 20170055485, 20170055486, 20170055487, 20170055488, 20170055489, 20170055490, 20170056038, 20170056039, 20170056040, 20170056041, 20170056042, 20170056043, 20170056044, 20170056045, 20170056046, 20170056047, 20170056048, 20170056049, 20170056050, 20170056051, 20170056052, 20170056053, 20170056054, 20170056055, 20170056056, 20170056527, 20170056528, 20170056529, 20170056530, 20170056531, 20170056532, 20170056533, 20170056534, 20170056535, 20170056536, 20170056537, 20170056538, 20170056539, 20170056540, 20170056541, 20170056542, 20170056543, 20170056544, 20170056545, 20170056546, 20170058170, 20170058171, 20170058172, 20170058173, 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510(k) numbers
not on file
PMA numbers
not on file
Product code
FNL
Firm FEI
3008058231
Firm city
Slany
Firm state
not on file
Firm country
Czech Republic

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

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

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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