← FDA ENFORCEMENT
Z-1002-2026Class I
AVID Medical, Inc.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
AVID Medical, Inc.
Product type
Device
Status
Ongoing
Report date
2026-01-14
Distribution
US Nationwide distribution in the states of FL, GA and Puerto Rico.
Firm state
VA
Product quantity
380 units
Initiated by
Voluntary: Firm initiated
Reason for recall
Devices are not suitable for organ transplant.
Product description
Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
Code / lot info
Kit Code: JACK097-08; UDI : 10809160462829; Lot No: 1654185.
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →