Medline Industries Inc.: Medical Device Recall in 2022 - (Recall #: Z-1683-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Medline CHEST TUBE REORDER NO: DYNJ36762A

Product Classification:

Class II

Date Initiated: July 21, 2022

Date Posted: September 14, 2022

Recall Number: Z-1683-2022

Event ID: 90689

Reason for Recall:

Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit

Status: Ongoing

Product Quantity: 300 kits

Code Information:

Model Number: DYNJ36762A UDI-DI Code (GTIN Insert/GTIN Case / Lot Number: (01)1019348989440/(01)40193489894401 / 21ILA164 (01)1019348989440/(01)40193489894401 / 21ILA986 (01)1019348989440/(01)40193489894401 / 21JLA315 (01)1019348989440/(01)40193489894401 / 21KLA005 (01)1019348989440/(01)40193489894401 / 21KLA162 (01)1019348989440/(01)40193489894401 / 21KLA629

Distribution Pattern:

U.S. Nationwide distribution in the state of AL.

Voluntary or Mandated:

Voluntary: Firm initiated