Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH
Reported: February 26, 2020 Initiated: December 20, 2019 #Z-1239-2020
Product Description
Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH
Reason for Recall
Product lidstock contains the incorrect expiration date for the product
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- 1150 units
- Distribution
- Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH. Recalled by Arrow International Inc. Units affected: 1150 units.
Why was this product recalled? ▼
Product lidstock contains the incorrect expiration date for the product
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 26, 2020. Severity: Moderate. Recall number: Z-1239-2020.
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