Vascular Solutions, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1250-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer kit is intended to facilitate the percutaneous placement of guidewires in the vascular system and for delivery of contrast media to vascular sites.

Product Classification:

Class II

Date Initiated: January 12, 2017

Date Posted: March 1, 2017

Recall Number: Z-1250-2017

Event ID: 76363

Reason for Recall:

Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires that have a shelf life shorter than the kit expiration date.

Status: Terminated

Product Quantity: 633

Code Information:

Lot Numbers: 581212, 584392, 594115, 597202

Distribution Pattern:

US Nationwide Distribution in the states of NH, ME, VT, NY, LA, MS, AL CA, IA, WA, OR, MD, DE, PA, NJ, ID, TX, OK, MO, WI, GA, FL, AR, OH, AZ.

Voluntary or Mandated:

Voluntary: Firm initiated