AVID Medical Recalls Halyard IV Start Kits Due to Packaging Seal Issues
AVID Medical is recalling Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a packaging defect (open or incomplete seal) without reported injuries or illnesses, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
AVID Medical, Inc. is recalling Halyard IV Start Kits, Non-Sterile, Model Number KRIV26-02. The recall involves 816 kits (17 cases) that were distributed nationwide in the United States. The kits contain a BD ChloraPrep Clear 1 mL Applicator.
The recall is being conducted because the packaging of the BD ChloraPrep applicator may exhibit an open or incomplete seal. Specific lot numbers affected include 1658438, 1685838, 1699753, and 1706455.
Healthcare facilities and consumers should check their inventory for the affected model number and lot numbers. If the product is found, it should be removed from use and returned to the distributor or manufacturer according to their instructions.
The recalled product
- Product
- Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02
- Manufacturer
- AVID Medical, Inc.
- Category
- Medical Device — IV Start Kits
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- 1685838 (12/19/2027)
- 1699753 (02/28/2027)
- 1706455 (12/19/2027).
Distribution
Distributed nationwide across the United States.
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