MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2025 - (Recall #: Z-0780-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYNJ910120

Product Classification:

Class II

Date Initiated: November 21, 2024

Date Posted: January 8, 2025

Recall Number: Z-0780-2025

Event ID: 95852

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.

Status: Ongoing

Product Quantity: 74 units

Code Information:

1) REF DYNJ69476, UDI/DI 10193489947786 (EA) 40193489947787 (CS), Lot Numbers: 21HDB296; 2) REF DYNJ910120, UDI/DI 10195327589202 (EA) 40195327589203 (CS), Lot Numbers: 24CMH776.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated