FLEXTIP PLUS EPIDURAL CATHETER recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIOngoing
Summary: ARROW INTERNATIONAL, LLC is recalling FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 The Arrow Epidural Catheter kit permits access to the epidural space for administration of epidural anesthetic. The epidura. Reason: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured.
What is being recalled
FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 The Arrow Epidural Catheter kit permits access to the epidural space for administration of epidural anesthetic. The epidural catheter kit is intended for use up to 72 hours. The Arrow Combined Spinal Anesthesia and Epidural Catheterization products permit access to subarachnoid and epidural spaces. The Arrow Single Shot Epidural product permits access to the epidural space..
Why
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA. (states named: Arizona, California, Georgia, Massachusetts, Maine, Michigan, Oregon, Pennsylvania, Virginia)
How to tell if yours is affected
Product code:ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 Batch Number: 33F25K0409
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1913-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | March 11, 2026 |
| Reported | April 29, 2026 |
| Company | ARROW INTERNATIONAL, LLC |
| Company location | Morrisville, NC, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 190 |
More recalls from ARROW INTERNATIONAL, LLC · all medical device recalls · recalls from March 2026