MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2024 - (Recall #: Z-0154-2025)

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) SET UP PACK, REF DYNJ36320A; b) ANGIOGRAM WRO-LF, REF DYNJ41876B

Product Classification:

Class II

Date Initiated: September 4, 2024

Date Posted: October 30, 2024

Recall Number: Z-0154-2025

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: 312 units

Code Information:

a) DYNJ36320A, UDI/DI 40889942245230 (each), 10889942245239 (case), Lot Numbers: 24ABC836; b) DYNJ41876B, UDI/DI 40193489563086 (each), 10193489563085 (case), Lot Numbers: 23LBM850

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated