Lower riskMedical device recall · FDA · Published May 7, 2026
AVID Medical Halyard EYE PACK Recall: Incorrect Betadine Concentration
AVID Medical recalls Halyard EYE PACK convenience kits with model LVEY27 due to incorrect Betadine solution concentration. Affected units have specific lot numbers and expiration dates.
“AVID Medical Halyard EYE PACK Recall: Incorrect Betadine Concentration.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/128008-avid-medical-halyard-eye-pack-recall-incorrect-betadine-concentration. Based on FDA recall #Z-2763-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2763-2026%22&limit=1).
AVID Medical, Inc. has voluntarily recalled Halyard EYE PACK convenience kits due to an incorrect concentration of Betadine solution, the FDA said on May 7, 2026. The recall affects 260 kits distributed in California.
How to tell if you have it
Brand: AVID Medical
Product: Halyard EYE PACK Convenience kit
Model/Catalog Number: LVEY27
UDI-DI: 10809160499528
Lot Numbers: 1680076 (Expiration Date: 12/31/2026), 1680590 (Expiration Date: 6/30/2027)
Distribution: US Nationwide distribution in the state of California
The hazard
The recalled kits contain an incorrect concentration of Betadine solution. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show AVID Medical, Inc. has had 23 other recalls on record since June 22, 2017. Other recent recalls by the brand include Halyard UNIV IMAGING BIOPSY TRUCUSTOM kits recalled on Aug. 10, 2026, and Halyard IV Start Kits recalled on July 22, 2026. Other recent recalls of similar products include Medline Eye Kits recalled on June 12, 2026, Medline Ophthalmic Packs with Lidocaine recalled on May 21, 2026, and Medline EYE TRAY-LF Kit recalled on April 10, 2026.
How to tell if you have this one
Check for the model number LVEY27 on the Halyard EYE PACK convenience kit. Lot numbers 1680076 (expiring 12/31/2026) or 1680590 (expiring 6/30/2027) are affected.
Brand
AVID Medical
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the model number LVEY27 and lot numbers 1680076 or 1680590 on the Halyard EYE PACK convenience kit.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution in the state of California.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2763-2026 (May 7, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2763-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.