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FDA Medical Device Recalls (openFDA)

MEDLINE INDUSTRIES, LP - Northfield: Centurion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray

Recall number
Z-1917-2024
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Product
Centurion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray
Status
Open, Classified
Initiated
2024-03-01
Posted
2024-05-29
Terminated
not on file
Reason
Trumpet Needle Guide ring can detach when excessive pressure is applied.
Root cause
Process control
Action
Medline issued a correction notice to its consignees on 03/01/2024 via email and USPS first class mail. The notice explained the issue and requested the consignee identify and quarantine all affected products, and respond to the notice. Once the response was received Medline would provide labels to place over the affected product in stock. If the product was further distributed the party which distributed the product was directed to notify their customers.
Quantity
30 units
Distribution
US Nationwide distribution.
Lot, serial or model codes
UDI/DI 40653160122945 (case), 10653160122944 (unit), Lot Numbers: 23JBX257, 23KMG455
510(k) numbers
not on file
PMA numbers
not on file
Product code
LRP
Firm FEI
1417592
Firm city
Northfield
Firm state
IL
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

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