Galt Medical Corporation: 9 recalls on record

Recalls filed with 1 agency: FDA (9).

First recall on record: September 10, 2014. Most recent: August 19, 2026.

Risk classification: Class II: 9

Most recent recalls

DateAgencyProduct
August 19, 2026FDABoston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075…Z-2917-2026
May 14, 2025FDAB Braun Interventional Coaxial Dilator REF: KIT-018-47, KIT-019-67, KIT-018-41, KIT-…Z-1732-2025
May 14, 2025FDAGALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedu…Z-1734-2025
June 21, 2023FDATearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16Z-1968-2023
August 8, 2018FDA1) Drainer Centesis Catheter, Sterile EO, Rx Only, Catalog #: a) DRC-001-05, b) DRC-001…Z-2560-2018
August 8, 2018FDATearaway Introducers, Catalog #: a) BNS-000-07, b) BNS-000-10; c) DIL-015-50; d) DS…Z-2565-2018
August 8, 2018FDACenteze Centesis Catheter, Catalog #: a) DRC-006-05, b) DRC-006-15,Z-2563-2018
September 10, 2014FDAGALT VALVED TEARAWAY INTRODUCER SET GALT VTI RX ONLY UNITS 7 STERILE EO Product…Z-2588-2014
September 10, 2014FDAGALT VALVED TEARAWAY KIT GALT VTI w/ Sideport Stainless Steel Dbl Flex. J-St RX ONLY U…Z-2589-2014

Questions about this company

How many recalls does Galt Medical Corporation have?
Recalert has 9 U.S. recalls on record for Galt Medical Corporation, published between September 10, 2014 and August 19, 2026.
What was the most recent Galt Medical Corporation recall?
FDA recall Z-2917-2026, published August 19, 2026: Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator , Stiffen Dilator, Nitinol Mandrel Wire w/ Radiopaque Tip [Au}, Needle, Extension Tu…
Which agencies have handled Galt Medical Corporation recalls?
Galt Medical Corporation appears as the recalling firm in recalls from: FDA (9).

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