Arrowg+ard Blue Advance JACC Recalled for Incorrect Expiration Date
Arrow International Inc. is recalling 77 units of Arrowg+ard Blue Advance JACC products because they were labeled with an incorrect expiration date.
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 specific defect is a minor labeling error (incorrect expiration date) with no reported injuries or illnesses, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Arrow International Inc. is recalling 77 units of Arrowg+ard Blue Advance JACC products, identified by Product Code CDC 41552 JX1A. The recall is due to the products being labeled with an incorrect expiration date.
The affected products were distributed nationwide and to foreign markets. The specific batch codes involved are 23F17K0694 and 23F18K0108.
Consumers who have these products should check the expiration date and batch code. If the product matches the recalled description, they should stop using it and contact the manufacturer for instructions.
The recalled product
- Product
- Arrowg+ard Blue Advance JACC Product Code: CDC 41552 JX1A
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — Syringes
- Hazard
- Affected units
- 77
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 (2)
- Batch Code: 23F17K0694
- 23F18K0108
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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