Arrowg+ard Blue Advance JACC Recalled for Incorrect Expiration Date
Arrow International Inc is recalling Arrowg+ard Blue Advance JACC products due to an incorrect expiration date. The recall involves 174 units distributed nationwide.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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, but the hazard is a labeling error (incorrect expiration date) with no reported illnesses or injuries, fitting the 'Moderate' criteria for minor labeling errors.
Plain-English summary
Arrow International Inc is voluntarily recalling Arrowg+ard Blue Advance JACC products, identified by product code CDC 42063 JX1A and batch code 23F17C0488. The recall was initiated because the products were labeled with an incorrect expiration date.
A total of 174 units are affected by this recall. The products were distributed nationwide and to foreign markets. The source text does not specify which specific foreign countries were involved.
Consumers who have these products should check the expiration date and contact Arrow International Inc for further instructions or a refund. No illnesses or injuries have been reported in connection with this recall.
The recalled product
- Product
- Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — Infusion Pumps
- Hazard
- Affected units
- 174
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 (1)
- Batch Code: 23F17C0488
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 36 recalled by Arrow International Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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