FDA Device recall Z-3023-2026
Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M
- FDA Device
- Class II
- ongoing
- Published 2026-09-02
On 2026-09-02 the FDA classified a Class II recall of Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M by Medline Industries, citing kits contain a potentially contaminated component which were recalled by the manufacturer.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3023-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-10 |
| Published | 2026-09-02 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M
Reason
Kits contain a potentially contaminated component which were recalled by the manufacturer
Identifiers
| code_info | UDI/DI 10198459447327 (each) 40198459447328 (case), kit lot number 25JBE079. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3023-2026%22
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