FDA Device Recalls

Recalls /

#214675

Product

Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: LABOR TRIAGE KIT, REF DYKM1564

FDA product code
LROGeneral Surgery Tray
Device class
Class 2
Medical specialty
General, Plastic Surgery
Affected lot / code info
UDI/DI 10889942754571 (EA), 40889942754572 (CASE), Lot Numbers: 24EBR566

Why it was recalled

Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.

Root cause (FDA determination)

Other

Action the firm took

On June 12, 2025, firm instructed customers to request stickers to over-label the affected convenience kits with a warning label indicating to remove the affected component and replace it with product from supply. No product is to be returned.

Recalling firm

Firm
MEDLINE INDUSTRIES, LP Northfield
Address
3 Lakes Dr, Northfield, Illinois 60093-2753

Distribution

Distribution pattern
Distributed domestically to California, Florida, Pennsylvania, and Texas. No international distribution.

Timeline

Recall initiated
2025-06-12
Posted by FDA
2025-07-21
Status

Source: openFDA Device Recall endpoint. Recall record ID #214675. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.