MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2025 - (Recall #: Z-0719-2025)

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:

DIEP FLAP Convenience kit, SKU DYNJ910120. Convenience kits used for various procedures.

Product Classification:

Class II

Date Initiated: November 6, 2024

Date Posted: January 1, 2025

Recall Number: Z-0719-2025

Event ID: 95806

Reason for Recall:

Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods

Status: Ongoing

Product Quantity: 26 kits

Code Information:

UDI-DI: 10195327589202(each), 40195327589203(case); Lot Number: 24CMH776

Distribution Pattern:

US Nationwide. Canada.

Voluntary or Mandated:

Voluntary: Firm initiated