Galt Medical Corporation recalls

7 recalls on record · latest: March 27, 2025

Official U.S. recall history for Galt Medical Corporation, compiled from official government records.

Get recall alerts

Free email alert whenever Galt Medical Corporation has a new recall — straight from official government data. Unsubscribe anytime.

Galt Medical Corporation recalls GALT Centeze Catheter REF: DRC-002-05 DRC-002-06 The Centeze is intended for use in percutaneous fluid aspirations and…

March 27, 2025 · Medical device recalls Moderate risk Due to a potential open seal in the sterile barrier packaging .

Galt Medical Corporation recalls Introducer Kit- Coaxial Dilator REF: KIT-002-28, 00841268104730 KIT-002-34, 00841268104792 KIT-002-35, 00841268104808 K…

March 27, 2025 · Medical device recalls Moderate risk Due to a potential open seal in the sterile barrier packaging.

Galt Medical Corporation recalls Introducer Needle REF NDL-107-04 These needles are used for the percutaneous introduction of guidewires

March 27, 2025 · Medical device recalls Moderate risk Due to a potential open seal in the sterile barrier packaging.

Galt Medical Corporation recalls Introducer Kit- Tearaway MicroSlide REF KIT-051-01, 00841268106130 INT-101-15, 00841268107380 These introducers are use…

March 27, 2025 · Medical device recalls Moderate risk Due to a potential open seal in the sterile barrier packaging.

Galt Medical Corporation recalls B Braun Interventional ELITE HV Hemostasis Valve Introducer System REF 612802 Model Number: BCL-100-04 The Elite HV¿ In…

March 27, 2025 · Medical device recalls Moderate risk Due to a potential open seal in the sterile barrier packaging .

Galt Medical Corporation recalls B Braun Interventional Coaxial Dilator REF: KIT-018-47, KIT-019-67, KIT-018-41, KIT-019-37 These Micro-Introducer Kits…

March 27, 2025 · Medical device recalls Moderate risk Due to a potential open seal in the sterile barrier packaging .

Galt Medical Corporation recalls GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to introduce and position cat…

March 27, 2025 · Medical device recalls Moderate risk Due to a potential open seal in the sterile barrier packaging.