MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2025 - (Recall #: Z-1619-2025)

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 Convenience kits used for various procedures: 1) ARTHROSCOPIE DU GENOU-LF, Model Number: DYNJ40229A; 2) ARTHROSCOPY PACK-LF, Model Number: OPK382N; 3) ARTHROSCOPY NEW TEGH-LF, Model Number: DYNJ46723B

Product Classification:

Class II

Date Initiated: March 3, 2025

Date Posted: April 23, 2025

Recall Number: Z-1619-2025

Event ID: 96510

Reason for Recall:

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Status: Ongoing

Product Quantity: 222 units

Code Information:

1) DYNJ40229A, UDI-DI: 10889942670482(each), 40889942670483(case), Lot Number: 24JBM438; 2) OPK382N, UDI-DI: 10889942686704(each), 40889942686705(case), Lot Number: 24JBN001; 3) DYNJ46723B, UDI-DI: 10889942747405(each), 40889942747406(case), Lot Number: 24JBQ891

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated