FDA recall, , Moderate risk
AVID Medical Halyard IV Start Kits
Halyard IV Start Kit NON-Sterile may have an open or incomplete seal on the applicator packaging.
Summary by Recall Canary from the FDA notice
What happened
AVID Medical, Inc., of Toano, Virginia, recalled Halyard IV Start Kit Non-Sterile convenience kits containing BD ChloraPrep Clear - 1 mL Applicator because the applicator packaging may exhibit an open or incomplete seal. The recall began July 22, 2026, and was added to the FDA's Enforcement Report on September 23, 2026, with US Nationwide distribution. The affected kits are the Halyard IV Start Kit Non-Sterile containing BD ChloraPrep Clear - 1 mL Applicator.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
A UDI-DI is the device identifier printed with the barcode on the device label.
48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit
- Model
- KRIV26-02
- UDI-DI
- 10809160460481
- Model
- KRIV26-01
- UDI-DI
- 10809160450109
- Lot code
- 1642214
Some entries omit identifying details. Check the notice to confirm which units are affected.
Recall details
- Company began the recall
- Sold in
US Nationwide distribution.
- Company
- AVID Medical, Inc.Toano, Virginia
- Hazard
- Packaging defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99764
- Recall numbers
- Z-3260-2026 to Z-3261-2026
All recalls from AVID Medical, Inc.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
