MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2024 - (Recall #: Z-0171-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Medline brand medical procedure convenience kits, labeled as: a) UNIVERSAL DRAPE PACK, REF DYNJ44114; b) DRAPE PACK, REF DYNJ82663B

Product Classification:

Class II

Date Initiated: September 4, 2024

Date Posted: October 30, 2024

Recall Number: Z-0171-2025

Event ID: 95415

Reason for Recall:

It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.

Status: Ongoing

Product Quantity: 194 units

Code Information:

a) REF DYNJ44114, UDI/DI 40888277202055 (each), 10888277202054 (case), Lot Numbers: 24ABB398; b) REF DYNJ82663B, UDI/DI 40195327544325 (each), 10195327544324 (case), Lot Numbers: 23LBV498

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated