FDA · Medical devices ·
Halyard IV Start Kit Non-Sterile REF: KRIV26-02 recall
AVID Medical, Inc. recalled Halyard IV Start Kit Non-Sterile REF: KRIV26-02 on September 16, 2026 because of convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area. It was sold nationwide.
Why it was recalled
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.
What's recalled
Halyard IV Start Kit Non-Sterile REF: KRIV26-02
Quantity: 98 Kits
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- AVID Medical, Inc., Toano, VA
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution in the state of NE. - Status
- Ongoing
- Recall number
- Z-3109-2026
- Source
- U.S. Food and Drug Administration
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