FDAClass II · Medical device · Recall Z-1917-2026 · Recalled April 29, 2026
Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7 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
Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 The MAC Multi-Lumen Central Venous Access Device with Arrowg+ard Blue technology permits short-term (<30 days) venous access and catheter introduction to the central circulation. It may be inserted into the jugular, subclavian, or femoral veins. The Arrowg+ard technology is intended to help provide protection against catheterrelated infections. Clinical data have not been collected that demonstrate the use of the Arrowg+ard antimicrobial surface in decreasing catheter-related infections for this device. It is not intended to be used as a treatment for existing infections, nor is it indicated for long-term use.
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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: Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7 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 ↗
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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.