FDAClass II · Medical device · Recall Z-3109-2026 · Recalled September 16, 2026
Halyard IV Start Kit Non-Sterile REF recall — AVID Medical, Inc.
Agency report date: September 16, 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
Halyard IV Start Kit Non-Sterile REF: KRIV26-02
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: Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.
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: Halyard IV Start Kit Non-Sterile REF 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 AVID Medical recalls
- Halyard IV START KIT NON-STERILE recall — AVID Medical, Inc.FDA · September 30, 2026
- Haylard UNIV IMAGING BIOPSY TRUCUSTOM recall — AVID Medical, Inc.FDA · September 23, 2026
- Haylard BASIC BIOPSY TRAY recall — AVID Medical, Inc.FDA · September 23, 2026
- Haylard CONTINUOUS NERVE BLOCK TRAY recall — AVID Medical, Inc.FDA · September 23, 2026
- Haylard 18G SINGLE SHOT EPI TRAY recall — AVID Medical, Inc.FDA · September 23, 2026
Other medical device recalls from around the same time
- DuoGlide Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.FDA · September 23, 2026
- Power-Trialysis Short-Term Straight Dialysis Catheter recall — Bard Access Systems, Inc.FDA · September 23, 2026
- Kit recall — Medical Action Industries, Inc. 306FDA · September 16, 2026
- Kit recall — Medical Action Industries, Inc. 306FDA · September 16, 2026
- Bravo CF capsule delivery device recall — Given Imaging Ltd.FDA · September 16, 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 October 22, 2026 at 6:00 PM UTC.