FDA Device recall Z-2175-2023
Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) CATHETER INSERTION KIT CLABSI, Model Number CVI4880
- FDA Device
- Class II
- ongoing
- Published 2023-07-26
On 2023-07-26 the FDA classified a Class II recall of Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) CATHETER INSERTION KIT CLABSI, Model Number CVI4880 by Medline Industries Northfield, citing probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2175-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-05-18 |
| Published | 2023-07-26 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) CATHETER INSERTION KIT CLABSI, Model Number CVI4880; b) CENTRAL CATHETER INSERTION TRA, Model Number CVI680C; c) CVL INSERTION TRAY, Model Number DYNDC1786A; d) UNIVERSAL INSERTION KIT, Model Number ECVC1655; e) CVC INSERTION ACCESSORY KIT, Model Number ECVC7880; f) ULTASOUND GUIDED PIV INSERTION, Model Number IVS3635B
Reason
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Identifiers
| code_info | all lots within expiry, distributed from Medline between December 2017 - May 2023: Model Number CVI4880, UDI/DI (EA)…all lots within expiry, distributed from Medline between December 2017 - May 2023: Model Number CVI4880, UDI/DI (EA) 10195327233976, UDI/DI (CS) 40195327233977; Model Number CVI680C, UDI/DI (EA) 10653160992943, UDI/DI (CS) 40653160992944; Model Number DYNDC1786A, UDI/DI (EA) 10193489199116, UDI/DI (CS) 40193489199117; Model Number ECVC1655, UDI/DI (EA) 10653160254935, UDI/DI (CS) 40653160254936; Model Number ECVC7880, UDI/DI (EA) 10195327129613, UDI/DI (CS) 40195327129614; Model Number IVS3635B, UDI/DI (EA) 10653160992660, UDI/DI (CS) 40653160992661 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2175-2023%22
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