Arrow JACC Central Catheter Recalled for Incorrect Expiration Date
Arrow International Inc is recalling 191 units of JACC central catheters because the expiration date printed on the product is incorrect.
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 involves a labeling error (incorrect expiration date) without reported injuries or illnesses, fitting the criteria for a moderate severity recall.
Plain-English summary
Arrow International Inc is recalling 191 units of Arrow JACC with Chloraguard Technology Jugular Axillo subclavian Central Catheters. The recall was initiated because the expiration date listed on the product is incorrect.
The affected product is identified by Product Code CDC 42563 JX1A and Batch Codes 23F17E0686 and 23F18H0290. The recall is classified as Class II by the FDA.
Healthcare providers and consumers should stop using the affected catheters and contact Arrow International Inc for further instructions or a replacement.
The recalled product
- Product
- Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillo subclavian Central Catheter Product Code: CDC 42563 JX1A
- Manufacturer
- Arrow International Inc
- Hazard
- Affected units
- 191
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: 23F17E0686
- 23F18H0290
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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