Arrowg+ard Blue Advance JACC recalled for incorrect expiration date
Arrow International Inc is recalling 84 units of Arrowg+ard Blue Advance JACC due to incorrect expiration dates.
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, and the hazard is a minor labeling error (incorrect expiration date) with no reported injuries or illnesses.
Plain-English summary
Arrow International Inc is recalling 84 units of Arrowg+ard Blue Advance JACC, Product Code CDC 42052 JX1A. The recall was initiated because the product was labeled with an incorrect expiration date.
The affected units are identified by Batch Codes 23F18E0046 and 23F18J0269. The products were distributed nationwide and to foreign locations.
Consumers should stop using the affected products and contact Arrow International Inc for further instructions.
The recalled product
- Product
- Arrowg+ard Blue Advance JACC Product Code:CDC 42052 JX1A
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — Infusion Pumps
- Hazard
- Affected units
- 84
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: 23F18E0046
- 23F18J0269
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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