FDAFDA · Food and drugs·Recall number Z-1239-2020
Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH
Published February 26, 2020 · Recall initiated: December 20, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Product lidstock contains the incorrect expiration date for the product
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Arrow International Inc
- Distributor
- Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
- Lot
- Lot Number: 13F18A0714
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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