Galt Medical Corporation: Medical Device Recall in 2025 - (Recall #: Z-1737-2025)

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:

Introducer Kit- Tearaway MicroSlide REF KIT-051-01, 00841268106130 INT-101-15, 00841268107380 These introducers are used for the procedures to introduce catheters and other intravascular devices into the coronary and peripheral vasculature of adult and pediatric patients of all ages.

Product Classification:

Class II

Date Initiated: March 27, 2025

Date Posted: May 14, 2025

Recall Number: Z-1737-2025

Event ID: 96622

Reason for Recall:

Due to a potential open seal in the sterile barrier packaging.

Status: Ongoing

Product Quantity: 490 units

Code Information:

Catalog Number: KIT-051-01, UDI-DI code: 00841268106130 Lot Numbers: 24298473 24190504 INT-101-15, UDI-DI code: 00841268107380 Lot Number: 24284447

Distribution Pattern:

Worldwide - U.S. Nationwide distribution in the states of AL, FL, GA, IL, MA, OH, PA, and UT. The countries of Canada, Ireland, Israel, Korea, Qatar, and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated