Halyard IV START KIT NON-STERILE REF: KRIV26-02
FDA Recall Z-3108-2026 · Posted 2026-09-14
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Recalling FirmAVID Medical, Inc.
Recall StatusOpen, Classified
Product CodeLRO
Date Initiated2026-07-14
Product Quantity288 units
Reason for Recall
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides
Firm Action
On August 18, 2026, Avid Medical Inc. a subsidiary of Owens Minor issued an "Urgent Medical Device Recall Update" to affected consignees via email. The update was due to a revise recall strategy. Initial notification was sent on July 14, 2026. Avid ask consignees to take the following actions:
1. Identify, segregate, and quarantine all impacted product identified in TABLE 1.
2. Discontinue use of the BD ChloraPrep Clear - 1 mL and FREPP" Clear 1.5 mL Applicators.
3. FOR AVID KIT KRIV26-02, IV START KIT NON-STERILE, KIT LOT 1658437: Discard entire kit as it contains the contaminated component BD ChloraPrep" Clear - 1 mL, BD LOT 4032183.
4. Customers (end-users): If you received product from a distributor, please contact the distributor or your sales representative with any questions you may have.
5. Distributors: If any of the affected kits identified above were further distributed, please ensure all end-users are appropriately notified of the actions to take and maintain records of effectiveness.
6. Complete the attached Recall Response Form and return by August 28, 2026.
If you have any questions, contact Manager, Regulatory Affairs at 470-280-4277.
Root Cause
Packaging process control
Distribution Pattern
US Nationwide distribution in the state of NE.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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