FDAClass II · Medical device · Recall Z-1913-2026 · Recalled April 29, 2026
FLEXTIP PLUS EPIDURAL CATHETER recall — ARROW INTERNATIONAL, LLC
Agency report date: April 29, 2026.
1. Compare your item
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Agency product description and boundaries
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..
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
2. Agency hazard and consumer action
FDA reports: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.
Class II: may cause temporary or medically reversible health consequences.
Affected product: FLEXTIP PLUS EPIDURAL CATHETER recall status
3. Open the official notice or contact
View the official FDA enforcement record (openFDA) ↗
Affected products
Companies & origin
Identifying details (verbatim from the notice)
Related recalls
More ARROW INTERNATIONAL recalls
- Description/REF recall — ARROW INTERNATIONAL, LLCFDA · June 24, 2026
- Description/REF recall — ARROW INTERNATIONAL, LLCFDA · June 24, 2026
- Description/REF recall — ARROW INTERNATIONAL, LLCFDA · June 24, 2026
- Description/REF recall — ARROW INTERNATIONAL, LLCFDA · June 24, 2026
- Description/REF recall — ARROW INTERNATIONAL, LLCFDA · June 24, 2026
Other medical device recalls from around the same time
- AIDBAGs are first aid kits of convenience composed of individually labeled devices designe recall — North American Rescue LLC.FDA · May 6, 2026
- WHILL Model F recall — WHILL, INC.FDA · May 6, 2026
- WHILL Model C2 recall — WHILL, INC.FDA · May 6, 2026
- Boston Scientific Cardiac Resynchronization Therapy (CRT)labeled as recall — Boston Scientific CorporationFDA · May 6, 2026
- Boston Scientific Pacemaker recall — Boston Scientific CorporationFDA · May 6, 2026
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
Found something wrong or missing? Report a data error.
Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved July 28, 2026 at 11:00 PM UTC.