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.
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 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.
See all 36 products in this recall →Related recalls
Same manufacturer · Arrow International Inc
See all →- HighArrow Arterial Kits Recalled Due to Open Packaging Seals
FDA (Devices) · 2024-10-02
- SevereIntra-Aortic Balloon Catheter Kit Recalled for Inflation and Structural Defects
FDA (Devices) · 2024-06-12
- SevereArrow Ultra 8 Intra-Aortic Balloon Catheter Kit Recalled for Inflation Defect
FDA (Devices) · 2024-06-12
- SevereArrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled for Device Malfunction
FDA (Devices) · 2024-06-12
- SevereARROW QuickFlash Radial Artery Catheters Recalled for Defective Component
FDA (Devices) · 2024-03-27
Same hazard · mis labeling
See all →- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-10-14
- SevereBetter Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk
FDA (Food) · 2026-10-14
- HighFreshPoint Recalls Cranberry Chicken Salad Wedges for Undeclared Egg Allergen
FDA (Food) · 2026-10-14
- HighJ K Patisserie & Bakery LLC Recalls Croissants for Undeclared Egg
FDA (Food) · 2026-10-14
- ModerateHalyard Laparoscopy Comprehensive Pack II Recalled for Latex Content
FDA (Devices) · 2026-10-14
Similar recalls
- ModerateArrow International Recalls PICC Sets with Incorrect Expiration Dates
FDA (Devices) · 2020-02-26
- ModerateArrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date
FDA (Devices) · 2020-02-26
- ModerateArrow International Recalls Central Venous Catheters With Incorrect Guide
FDA (Devices) · 2018-02-28
- ModerateArrow Central Venous Catheterization Kit Recalled for Incorrect Expiration Date
FDA (Devices) · 2020-02-26
- SevereFDA Recalls Arrow PICC Catheters with Incorrect Product Code Labels
FDA (Devices) · 2023-10-11
- ModerateArrow International Recalls Central Venous Catheterization Kits Due to Incorrect Guide
FDA (Devices) · 2018-02-28