Z-3023-2026 Class II Ongoing
FDA device recall Z-3023-2026 was initiated by Medline Industries, LP on Jul 10, 2026 and is designated Class II. Reason for recall: Kits contain a potentially contaminated component which were recalled by the manufacturer The recall status is ongoing. Affected quantity: 15 kits.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 2, 2026
- Initiation Date
- Jul 10, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 15 kits
Product Description
Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M
Reason for Recall
Kits contain a potentially contaminated component which were recalled by the manufacturer
Distribution Pattern
US Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI.
Code Information
UDI/DI 10198459447327 (each) 40198459447328 (case), kit lot number 25JBE079.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-3023-2026
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 24, 2026