FDA Medical devices recall ·
Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M recall
- Recall number
- Z-3023-2026
- Date
- (initiated July 10, 2026)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 15 kits
- Hazard tags
- Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M
Why was it recalled?
Kits contain a potentially contaminated component which were recalled by the manufacturer
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI/DI 10198459447327 (each) 40198459447328 (case), kit lot number 25JBE079.
Distribution
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.
States: Alabama California Florida Illinois Kansas Louisiana Massachusetts Maryland Missouri Mississippi Montana Nevada New York Ohio Oklahoma South Carolina Texas Wisconsin
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-3023-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.