Class II

Medical Device Recall: Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF

MEDLINE INDUSTRIES, LP - Northfield · November 21, 2024

Reason for Recall

Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

Distribution

Worldwide distribution - US Nationwide and the countries of UAE, and Canada.

States Affected

NATIONWIDE

Quantity Affected

128 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0791-2025

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 - Northfield Medical Device Recall: Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF | SafeCheck