Cardiohelp-i, blood oxygenation and carbon dioxide removal system, Part Numbers 701072780 (Cardiohelp-i), 701068550 (Slide Rail Holder)
FDA Recall Z-0290-2024 · Posted 2023-11-09
Recalling FirmMaquet Medical Systems USA
Recall StatusOpen, Classified
Product CodeDTQ
Date Initiated2023-10-12
Product Quantity1022 units
Reason for Recall
It was found that the fixation (weld) employed by the supplier of the nut bolt to the slide rail plate was insufficient. The deficient weld allows the nut bolt to break off from the slide rail plate with slight manual force.
Firm Action
An URGENT MEDICAL DEVICE Correction notification letter dated 10/12/23 was sent to customers.
Actions to be taken by the Customer:
Our records indicate that you have received a CARDIOHELP-i System having a serial number
that is affected by this voluntary Medical Device Correction.
" Please examine your inventory immediately to determine if you have any affected
CARDIOHELP System(s) in your inventory.
" Should you have any affected CARDIOHELP-i System(s), your unit(s) will need to be
returned to Getinge for correction. Getinge will contact your facility to arrange the return
of your unit for correction. A CARDIOHELP loaner can be provided if needed.
" Please do not to fixate any accessory at the slide rail until the slide rail holders
have been replaced.
" Affected CARDIOHELP-i can be used for intra-hospital transport only when placed
on a Sprinter cart.
" Inter-hospital transport is not permitted until the slide rail holders have been
replaced.
" Please forward this information to all current and potential CARDIOHELP-i users
within your hospital / facility.
" If you are a distributor who has shipped any affected products to customers, please
forward this document to their attention for appropriate action.
" Whether or not your facility has affected product(s) listed in this notice, please complete
and sign the attached MEDICAL DEVICE- CORRECTION RESPONSE FORM (Page 4) to acknowledge that you have received this notification. Return the completed form to
Getinge by e-mailing a scanned copy to [email protected] or by
faxing the form to 1-866-313-4049.
Type of Action by Getinge:
A Getinge representative will contact you to arrange for the repair of your CARDIOHELP -i
unit(s). Getinge will correct your CARDIOHELP -i unit(s) upon receipt and will return your unit(s)
once correction has been completed.
This voluntary correction only affects the products listed on Page 1; no other products are
affected by this voluntary correction.
We apologize for
Root Cause
Device Design
Distribution Pattern
US Nationwide.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.