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 listed by Lidstock.
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, but the specific defect is a labeling error (incorrect expiration date) without reported injuries or illnesses, fitting the criteria for a moderate severity labeling issue.
Plain-English summary
Arrow International Inc is recalling 96 units of Arrowg+ard Blue Advance JACC (Product Code: CDC 42041 JX1A) because the product was distributed with an incorrect expiration date. The recall is associated with Batch Code 23F18F0716.
The source text states that Lidstock identified the incorrect expiration date for the product. The affected units were distributed nationwide and to foreign locations.
Consumers should check their inventory for this specific product code and batch code. If the product is found, it should be returned to the point of purchase or the manufacturer for a refund or replacement.
The recalled product
- Product
- Arrowg+ard Blue Advance JACC Product Code: CDC 42041 JX1A
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — Infusion Pumps
- Hazard
- Affected units
- 96
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: 23F18F0716
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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