Halyard IV START KIT NON-STERILE REF: KRIV26-02
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides
- Agency
- FDA Device
- Recall date
- Jul 14, 2026
- Status
- Ongoing
- Company
- AVID Medical, Inc.
1. What product was recalled?
Halyard IV START KIT NON-STERILE REF: KRIV26-02
Halyard IV START KIT NON-STERILE REF: KRIV26-02
Quantity: 288 units
Code or lot text: Lot Number: 1658437 UDI: 10809160460481
- LOT
- Lot Number: 1658437 UDI: 10809160460481
- RECALL-NUMBER
- Z-3108-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Nationwide
View source evidence for state distribution
- Nebraska: US Nationwide distribution in the state of NE.
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. The Recall Guy's urgency label is urgent, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- created
10. Where is the official source?
Open the official FDA Device source
The Recall Guy normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.