Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation.
Reported: September 21, 2016 Initiated: February 17, 2016 #Z-2773-2016
Product Description
Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation.
Reason for Recall
Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- 6,121 units in total
- Distribution
- US Distribution to states of: NC, OH, FL, and MD.
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation.. Recalled by Arrow International Inc. Units affected: 6,121 units in total.
Why was this product recalled? ▼
Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 21, 2016. Severity: Moderate. Recall number: Z-2773-2016.
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