← FDA ENFORCEMENT
Z-2409-2026Class II
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
2026-06-17
Distribution
US Nationwide distribution in the state of Iowa.
Firm state
VA
Product quantity
72 kits
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental MonitoringReason for recall
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Product description
Halyard, Drape Pack. Kit Code: LMDP36-01.
Code / lot info
Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028
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 →