Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arrow FlexTip Plus Epidural Kit with NRFit Connector Recalled by Arrow International Inc Due to Nine complaints reported that the rotatable collar on...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Arrow International Inc directly.
Affected Products
Arrow FlexTip Plus Epidural Kit with NRFit Connector, catheter system, Product Codes (US) OT19TAGSK OT19TAGSKA OT19TAPSK OT19TCGLK Product Codes (OUS) AT-05501-NRF OT19HBPSS UM-05400-NRF ASK-05500-NRON EJ-05400-NRON OU-05500-NRON TU-05500-NRON 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.
Quantity: 109 eaches (US), 23,021 (OUS)
Why Was This Recalled?
Nine complaints reported that the rotatable collar on the filter had detached, causing a leak.
Where Was This Sold?
This product was distributed to 4 states: CA, DE, FL, MT
About Arrow International Inc
Arrow International Inc has 431 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report