AVID Medical Recalls Halyard IV Start Kits Due to Packaging Seal Issues
AVID Medical is recalling 192 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 seal defect that may compromise sterility or product integrity, but no specific injuries or illnesses are reported in the source text.
Plain-English summary
AVID Medical, Inc. is recalling 192 Halyard IV Start Kits (Model Number: KRIV26-01) due to a packaging defect. The kits contain a BD ChloraPrep Clear 1 mL Applicator, which may exhibit an open or incomplete seal on its packaging.
The affected product is distributed nationwide in the United States. The specific lot number is 1642214, and the expiration date is July 31, 2027. The kits are non-sterile and are sold in cases of 48.
Consumers who have purchased these kits should stop using them and contact AVID Medical, Inc. for further instructions or a refund. The recall is limited to the specific model and lot number identified in the notice.
The recalled product
- Product
- Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-01
- Manufacturer
- AVID Medical, Inc.
- Category
- Medical Device — IV Start Kits
Distribution
Distributed nationwide across the United States.
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