Skip to the content

FDA Medical Device Recalls (openFDA)

Smiths Medical ASD, Inc.: medex TranStar DPT w/Stopcock & 3cc Flush 10/EA, Product Code REF MX950SCFT

Recall number
Z-0193-2025
Recalling firm
Smiths Medical ASD, Inc.
Product
medex TranStar DPT w/Stopcock & 3cc Flush 10/EA, Product Code REF MX950SCFT
Status
Open, Classified
Initiated
2024-09-24
Posted
2024-10-23
Terminated
not on file
Reason
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within the TranStar Disposable Pressure Transducer or from a defect within the TranStar Disposable Pressure Transducer chip.
Root cause
Process control
Action
Smiths medical issued an URGENT MEDICAL DEVICE REMOVAL notice to its consignees on 09/24/2024 via traceable mailing. The notice explained the issue, potential risk, and requested the destruction of all affected product. Distributors were directed to forward the notice to their customers.
Quantity
10 units
Distribution
Worldwide distribution.
Lot, serial or model codes
UDI/DI 50351688503945 (case), 10351688503947 (pouch), Lot Numbers: 4277663
510(k) numbers
not on file
PMA numbers
not on file
Product code
DPT
Firm FEI
3012307300
Firm city
Minneapolis
Firm state
MN
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

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

Search this register