Abbott Vascular: Medical Device Recall in 2019 - (Recall #: Z-0960-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound devices).

Product Classification:

Class II

Date Initiated: July 3, 2018

Date Posted: March 6, 2019

Recall Number: Z-0960-2019

Event ID: 82015

Reason for Recall:

Incorrect expiration being entered for one lot.

Status: Terminated

Product Quantity: 26 units

Code Information:

Device Identifier #: 08717648 01360 7 Part Number: 1000185 Lot number: 60047593

Distribution Pattern:

US Nationwide Distribution - NC and NY

Voluntary or Mandated:

Voluntary: Firm initiated