Arrowg+ard Blue Advance JACC Recalled for Incorrect Expiration Date
Arrow International Inc. is recalling 52 units of Arrowg+ard Blue Advance JACC products due to an incorrect expiration date.
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 hazard is a labeling error (incorrect expiration date) with no reported illnesses or injuries, fitting the 'Minor labeling errors' criterion for a Moderate severity score.
Plain-English summary
Arrow International Inc. is recalling 52 units of Arrowg+ard Blue Advance JACC products (Product Code: JRT 43552 HPHNM, Batch Code: 13F18H0239). The recall was initiated because the product was labeled with an incorrect expiration date.
The affected units were distributed nationwide and to foreign markets. The source text does not specify the exact nature of the expiration date error or whether the products were expired or had a future date.
Consumers who possess these specific units should stop using them and contact the manufacturer for instructions on return or disposal. No illnesses or injuries have been reported in connection with this recall.
The recalled product
- Product
- Arrowg+ard Blue Advance JACC Product Code: JRT 43552 HPHNM
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — Infusion Pumps
- Hazard
- Affected units
- 52
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: 13F18H0239
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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