Ethicon Sarl, a Johnson & Johnson Company: Medical Device Recall in 2024 - (Recall #: Z-2407-2024)

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:

SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1963

Product Classification:

Class II

Date Initiated: June 11, 2024

Date Posted: July 24, 2024

Recall Number: Z-2407-2024

Event ID: 94831

Reason for Recall:

Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.

Status: Ongoing

Product Quantity: 39,010 units (All US)

Code Information:

Product Number: 1963; UDI/DI: 10705031003132 (primary), 20705031003139 (box of 10); Lot numbers:

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of India and Japan.

Voluntary or Mandated:

Voluntary: Firm initiated