FDA Medical devices recall ·
Halyard IV START KIT NON-STERILE recall
- Recall number
- Z-3261-2026
- Date
- (initiated July 22, 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
- 192 kits (4 cases)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-01
Why was it recalled?
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.
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 Model Number: KRIV26-01. UDI-DI: 10809160450109. Lot Number: 1642214. Expiration Date: 7/31/2027
Distribution
US Nationwide distribution.
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-3261-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.