Access Vascular recalls HydroPICC 4Fr Single Lumen kits with incorrect expiration dates that could expire before the labeled date, posing a risk of using expired catheters.
Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit.
Access Vascular is recalling HydroPICC 4Fr Single Lumen kits with model number 80001002 due to incorrect expiration dates on some catheters. Using these kits could lead to expired catheters that might not function properly or cause complications.
The catheters in these kits have incorrect expiration dates, meaning they may expire before the labeled date on the kit. This could lead to using expired catheters that might not function properly or cause complications during medical procedures.
Healthcare providers using the HydroPICC 4Fr Single Lumen kits with model number 80001002 are likely affected. Patients receiving care through these kits may be at risk if the catheters expire prematurely.
Check for model number 80001002 on the HydroPICC 4Fr Single Lumen kits. Look for lot numbers 11389279 or 11391525 on the kit packaging.
Verify the expiration date on the catheters matches the kit's labeled expiration date. If it does not, stop using the kit.
Model number 80001002 for HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit.
Lot numbers 11389279 and 11391525.
Check the kit packaging for lot numbers 11389279 or 11391525 and verify the catheter expiration date matches the kit's labeled expiration date.
We’ve drafted a message you can send Access Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-1130-2023 — Access Vascular Access Vascular Hello, I own a Access Vascular that is covered by recall Z-1130-2023 from Access Vascular. 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.
