AVID Medical recall: Halyard IV Start Kit Non-Sterile REF: KRIV26-02
AVID Medical, Inc. is recalling Halyard IV Start Kit Non-Sterile REF: KRIV26-02 because of a sterility problem – 98 Kits. The U.S. Food and Drug Administration published the recall on September 16, 2026; it began on July 14, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Halyard IV Start Kit Non-Sterile REF: KRIV26-02 |
| Brand | AVID Medical |
| Company | AVID Medical, Inc. |
| Type | Medical devices |
| Classification | Class II |
| Recall date | July 14, 2026 |
| Published by FDA | September 16, 2026 |
| Quantity | 98 Kits |
| Recall ID | 99525 |
Recalled products
- Halyard IV Start Kit Non-Sterile REF: KRIV26-02
- FDA recall number
- Z-3109-2026
- Codes, lots and dates
- Lot Number:1658438 7/31/2026 UDI: 10809160460481
- Quantity
- 98 Kits
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99525
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Toano, VA, United States
Why it was recalled
The problem: a sterility problem.
The reason the FDA lists: “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.”
Where it was sold
Nationwide. Distribution as the FDA records it: “US Nationwide distribution in the state of NE.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99525, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other AVID Medical recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Sep 30, 2026 |  AVID Medical recall: Halyard IV START KIT NON-STERILEMedical devices · 288 kits (6 cases) | Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminat… Most serious | FDA Class I |
| Sep 30, 2026 | AVID Medical recall: Halyard IV START KIT NON-STERILEMedical devices · 816 kits (17 cases); 192 kits (4 cases) | Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an op… Serious | FDA Class II |
| Sep 23, 2026 | AVID Medical recall: Halyard IV START KIT NON-STERILE REF: KRIV26-02Medical devices · 288 units | Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators whi… Most serious | FDA Class I |
| Sep 23, 2026 | AVID Medical recall: Haylard and 3 more productsMedical devices · 1640 kits; 80 kits; 240 kits; 340 kits | a sterility problem Most serious | FDA Class I |
| Sep 9, 2026 | AVID Medical recall: Halyard medical convenience kits labeled as: 1) ENT and 2 more productsMedical devices · 11763 kits; 16223 kits; 816 kits | a sterility problem Serious | FDA Class II |
| Sep 2, 2026 | AVID Medical recall: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK and 1 more productMedical devices · 45 kits; 63 kits; 78 kits; 120 Kits; 130 KITS | Labeling Deficiency: The medical kit labeling fails to identify that the statlock componen… Serious | FDA Class II |
| Aug 26, 2026 | AVID Medical recall: Halyard LAVH PACKMedical devices · 40 packs | The kit component was subjected to EO sterilization, contrary to the manufacturer recommen… Serious | FDA Class II |
About this recall
Is AVID Medical Halyard IV Start Kit Non-Sterile REF: KRIV26-02 recalled?
Yes. AVID Medical, Inc. recalled it on July 14, 2026; FDA published it September 16, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Because of a sterility problem. The reason given: 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.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.