Lower riskMedical device recall · FDA · Published May 19, 2026
AVID Medical Halyard STANDARD LINE INSERTION PACK recall: Silicone seal defect risks fluid
AVID Medical recalls Halyard STANDARD LINE INSERTION PACK model PVHM234-01 due to silicone seal defects that may cause fluid leakage or occlusion. Affected units include specific lot numbers with expiration dates.
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.
“AVID Medical Halyard STANDARD LINE INSERTION PACK recall: Silicone seal defect risks fluid.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/127949-avid-medical-halyard-standard-line-insertion-pack-recall-silicone-seal. Based on FDA recall #Z-2772-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2772-2026%22&limit=1).
AVID Medical, Inc. recalled Halyard STANDARD LINE INSERTION PACK kits due to defective silicone seals that may cause fluid leakage, the FDA said on May 19, 2026.
How to tell if you have it
Brand: AVID Medical
Product: Halyard STANDARD LINE INSERTION PACK
Model/Catalog Number: PVHM234-01
Lot Numbers (Expiration date): 1597314 (8/31/2026), 1599022 (5/31/2026)
Distribution: U.S. Nationwide distribution in the state of California
The hazard
Defects in the silicone seal may result in "doming" due to improper sealing, potentially leading to fluid occlusion or leakage.
Context
GovInfoNow's records show AVID Medical, Inc. has 23 other recalls on record since June 22, 2017. Other recent recalls of similar products include Medline Dialysis Kits Recall: Silicone Seal Issues May Cause Blood Product Leakage (Jan. 8, 2026), Medline Dialysis Kits Recall: Silicone Seal Issues May Cause Blood Flow Problems (Jan. 8, 2026) and Medline Dialysis Dressing Kits Recall: Silicone Seal Issues May Cause Blood Flow Problems (Jan. 8, 2026).
How to tell if you have this one
Check for the model number PVHM234-01 on the product. Affected units have specific lot numbers: 1597314 (expires 8/31/2026) and 1599022 (expires 5/31/2026).
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 PVHM234-01 and lot numbers 1597314 or 1599022 on the device.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “U.S. 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 2 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-2772-2026 (May 19, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2772-2026 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.