Arrow Select Kits (ASK), Maximal Barrier Precautions Kits (CDC) and Arterial Catheterization Kit (NA) with Biopatch Dressing
Reported: February 4, 2015 Initiated: January 9, 2015 #Z-1030-2015
Product Description
Arrow Select Kits (ASK), Maximal Barrier Precautions Kits (CDC) and Arterial Catheterization Kit (NA) with Biopatch Dressing
Reason for Recall
Certain product codes and lot numbers of Kits with Biopatch Dressing were packaged with the incorrect size Biopatch Dressing. No risk to patients is anticipated.
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- 4484
- Distribution
- US (nationwide) and PR.
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
Arrow Select Kits (ASK), Maximal Barrier Precautions Kits (CDC) and Arterial Catheterization Kit (NA) with Biopatch Dressing. Recalled by Arrow International Inc. Units affected: 4484.
Why was this product recalled? ▼
Certain product codes and lot numbers of Kits with Biopatch Dressing were packaged with the incorrect size Biopatch Dressing. No risk to patients is anticipated.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 4, 2015. Severity: Low. Recall number: Z-1030-2015.
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