Multi-Lumen Central Venous Catheterization Kit
Reported: October 22, 2014 Initiated: September 18, 2014 #Z-0076-2015
Product Description
Multi-Lumen Central Venous Catheterization Kit
Reason for Recall
Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- 65
- Distribution
- US Distribution including the states of MD, NC , LA , IN , OH, KY, CA , PA , NY and NV.
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
Multi-Lumen Central Venous Catheterization Kit. Recalled by Arrow International Inc. Units affected: 65.
Why was this product recalled? ▼
Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 22, 2014. Severity: Moderate. Recall number: Z-0076-2015.
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