Devices

Device Recall Epidural Needle

Model / Serial
Lot No. RF4044686, expiration date 2006-09
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
The recalled kits with the wrong epidural needle was distributed to the following direct accounts, to the following states in TN and TX
Product Description
ARROW EPIDURAL CATHETERIZATION KIT. Product No. MC-05001.
Manufacturer
Arrow International Inc
1 Event
- Recall of Device Recall Epidural Needle

Manufacturer

Arrow International Inc

Manufacturer Address
Arrow International Inc, 2400 Bernville Rd, Reading PA 19605-9607
Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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