Reported Mar 6, 2019 · Terminated
PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction…
Abbott Vascular
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Abbott Vascular · 26531 Ynez Rd · Temecula, CA · 92591-4630
Is this the product you have?
- PLUS 30 PRIORITY
- PACK Accessory Kit Product UsageIs 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)
- Lot codes and dates
- Device Identifier #: 08717648 01360 7
- Part Number1000185
- Lot number60047593
- Amount recalled
- 26 units
Where it was sold
Why it was recalled
Incorrect expiration being entered for one lot.
This product could cause temporary or reversible health problems — stop using it.
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