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FDA (Device enforcement)Recalled 2025-03-27class ii

Galt Medical Corporation: Introducer Kit- Coaxial Dilator REF: KIT-002-28, 00841268104730 KIT-002-34, 00841268104792 KIT-002-35, 00841268104808 KIT-011-40, 00841268105553 KIT-011-62, 00841268105614 KI

Hazard

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

Details from the source

Reason for recall: Due to a potential open seal in the sterile barrier packaging. Distribution: 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. Quantity: 4,280 kits Lot/code info: Catalog Number: KIT-002-28 UDI-DI code: 00841268104730 Lot Number: G25038156 KIT-002-34, UDI-DI code: 00841268104792 Lot Number: G25064259 KIT-002-35, UDI-DI code: 00841268104808 Lot Number: G25029077 KIT-011-40, UDI-DI code: 00841268105553 Lot Number: S25031227 KIT-011-62, UDI-DI code: 00841268105614 Lot Numbers: G25052163 G25080165 KIT-038-04, UDI-DI code: 00841268104556 Lot Number: G25092186 KIT-039-03, UDI-DI code: 00841268104587 Lot Numbers: G25050190 G25078192 KIT-039-13, UDI-DI code: 00841268106055 Lot Number: G25050202 KIT-081-02 / PS2-38, UDI-DI code: 00841268108394 Lot Number: G25056231

UPC codes

00841268104730, 00841268104792, 00841268104808, 00841268105553, 00841268105614, 00841268104556, 00841268104587, 00841268106055, 00841268108394

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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