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FDA Medical Device Recalls (openFDA)

SPS Sterilization, Inc: Edwards Lifesciences Femoral Venous Cannula, 18FR, resterilized.

Recall number
Z-3032-2018
Recalling firm
SPS Sterilization, Inc
Product
Edwards Lifesciences Femoral Venous Cannula, 18FR, resterilized.
Status
Terminated
Initiated
2018-03-07
Posted
not on file
Terminated
2018-11-27
Reason
The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.
Root cause
Labeling False and Misleading
Action
Customers were notified via letter on about 03/02/2018. Instructions included to review inventory for affected devices, arrange for their return to SPS Sterilization, and complete and return the Buisness Response Card. A follow up letter was sent to customer on about 03/07/2018 and included a description of the risk and hazard involved. Instructions remained the same.
Quantity
1 unit total
Distribution
US distribution to AZ, CA, FL, OH, PA, TX, VA, WV
Lot, serial or model codes
Code Number VFEM018-R; Lot Number 59740463; Serial Number 16704192017-01
510(k) numbers
["K140208"]
PMA numbers
not on file
Product code
DWF
Firm FEI
3005057969
Firm city
Nixa
Firm state
MO
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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