FDAFDA · Food and drugs·Recall number Z-2409-2026
Halyard, Drape Pack. Kit Code: LMDP36-01.
Published June 17, 2026 · Recall initiated: April 30, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- AVID Medical, Inc.
- Distributor
- US Nationwide distribution in the state of Iowa.
- Lot
- Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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