FDA recall Z-1237-2020
Arrow International Inc · Class II · device
Product
Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC
Reason for recall
Product lidstock contains the incorrect expiration date for the product
Distribution
Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
Key facts
- Status
- Terminated
- Initiation date
- 2019-12-20
- Report date
- 2020-02-26
- Termination date
- 2021-02-25
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Reading, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1237-2020