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 is recalling Halyard STANDARD LINE INSERTION PACK model PVHM234-01 because defects in the silicone seal can cause fluid leakage or blockage. This could lead to complications for users, especially in medical settings.
The silicone seal in the Halyard STANDARD LINE INSERTION PACK can develop a bulge ("doming") due to improper sealing. This defect may cause fluid to leak or become blocked, potentially leading to complications in medical procedures.
Healthcare professionals using this medical device are most likely affected. Patients using the device may also be at risk if the seal defect causes fluid leakage.
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).
Look for the model number PVHM234-01 and lot numbers 1597314 or 1599022 on the device.
The recall indicates a potential risk of fluid leakage or blockage due to seal defects, so it is not recommended for use until the remedy is applied.
The recall does not specify a remedy, so contact AVID Medical for guidance on next steps.
The product was sold with specific expiration dates: lot 1597314 expires 8/31/2026 and lot 1599022 expires 5/31/2026.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2772-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-2772-2026 from AVID Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
