Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1
Reported: February 26, 2020 Initiated: December 20, 2019 #Z-1236-2020
Product Description
Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1
Reason for Recall
Product lidstock contains the incorrect expiration date for the product
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- 250 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) Epidural Catheterization Kit ASK-05400-CA1. Recalled by Arrow International Inc. Units affected: 250 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-1236-2020.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11