Class II

Medical Device Recall: Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M

Medline Industries, LP · July 10, 2026

Reason for Recall

Kits contain a potentially contaminated component which were recalled by the manufacturer

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 Affected

NATIONWIDE

Quantity Affected

15 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3023-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Medline Industries, LP Medical Device Recall: Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M | SafeCheck