ARROW Epidural Needle Component (product number AN-05501). Epidural needles permit access to the epidural space and are used as a conduit for epidural catheter placement.
Reported: February 18, 2015 Initiated: January 5, 2015 #Z-1080-2015
Product Description
ARROW Epidural Needle Component (product number AN-05501). Epidural needles permit access to the epidural space and are used as a conduit for epidural catheter placement.
Reason for Recall
The product labeling does not specify the 5 year shelf life of the product.
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- 63022
- Distribution
- Distribution US Nationwide, Canada and Mexico.
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
ARROW Epidural Needle Component (product number AN-05501). Epidural needles permit access to the epidural space and are used as a conduit for epidural catheter placement.. Recalled by Arrow International Inc. Units affected: 63022.
Why was this product recalled? ▼
The product labeling does not specify the 5 year shelf life of the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 18, 2015. Severity: Moderate. Recall number: Z-1080-2015.
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