FDA Medical devices recall ·
Halyard, Drape Pack recall
- Recall number
- Z-2409-2026
- Date
- (initiated April 30, 2026)
- Company / brand
- AVID Medical, Inc.
9000 Westmont Dr, Toano, VA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 72 kits
- Hazard tags
- Sterility
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Halyard, Drape Pack. Kit Code: LMDP36-01.
Why was it recalled?
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028
Distribution
US Nationwide distribution in the state of Iowa.
States: Iowa
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2409-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.