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Abbott Vascular recalls PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction
Recalled March 6, 2019 · FDA recall Z-0960-2019 · Abbott Vascular
Hazard
Incorrect expiration being entered for one lot. · FDA Class II
Units
26 units
Sold at
US Nationwide Distribution - NC and NY
Description
Incorrect expiration being entered for one lot.
Product
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).
Manufacturer(s)
Abbott Vascular
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →