Arrow JACC Central Catheter Recalled for Incorrect Expiration Date
Arrow International Inc. is recalling 6 units of Arrow JACC Central Catheters because the expiration date is incorrect.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is for a documentation issue (incorrect expiration date) with no reported injuries or illnesses, fitting the 'Low' severity criteria for packaging or documentation problems.
Plain-English summary
Arrow International Inc. is recalling 6 units of Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central Catheters. The recall is due to an incorrect expiration date listed on the product.
The affected product has the batch code 23F18J0277. The distribution pattern is listed as nationwide and foreign.
Consumers should stop using the product and contact the manufacturer for further instructions.
The recalled product
- Product
- Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central Catheter Product Code: CDC 42552 JX1A
- Manufacturer
- Arrow International Inc
- Hazard
- Affected units
- 6
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: 23F18J0277
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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