Arrow FlexTip Plus Epidural Catheterization Kit Recalled for Incorrect Expiration Date
Arrow International Inc is recalling 250 units of the Arrow FlexTip Plus Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
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 on lidstock) with no reported injuries or illnesses, fitting the criteria for a Low severity recall.
Plain-English summary
Arrow International Inc is recalling 250 units of the Arrow FlexTip Plus(R) Epidural Catheterization Kit, model ASK-05400-CA1. The recall was initiated because the product lidstock contains the incorrect expiration date for the product.
The affected units are identified by Lot Number 13F18A0527. The products were distributed nationwide and in foreign countries including AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA.
Consumers and healthcare providers should stop using the affected products and contact Arrow International Inc for further instructions or a replacement.
The recalled product
- Product
- Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1
- Manufacturer
- Arrow International Inc
- Hazard
- Affected units
- 250
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)
- Lot Number: 13F18A0527
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 20 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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