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 80001001 due to incorrect expiration dates on some catheters. Using these kits could lead to expired catheters being used, which may not function properly and could cause complications.
The catheters in these kits have an expiration date that is earlier than the labeled expiration date of the kit. This means the catheters could expire before the kit's expiration date, potentially leading to improper function or complications if used.
Healthcare professionals who use the HydroPICC 4Fr Single Lumen kits with model number 80001001 are likely affected. Those using the recalled kits with specific lot numbers (11398679, 11416178) are at risk of using expired catheters.
Check for the model number 80001001 on the HydroPICC 4Fr Single Lumen kit. Look for lot numbers 11398679 or 11416178 on the product label.
Verify the kit's expiration date against the catheter expiration date to ensure they match the labeled expiration date.
The recall is due to some catheters in the kit having an incorrect expiration date that expires before the labeled expiration date of the kit.
Lot numbers 11398679 and 11416178 are affected.
The recall record does not specify a remedy, so check the expiration dates and ensure catheters do not expire before the kit's labeled 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-1131-2023 — Access Vascular Access Vascular Hello, I own a Access Vascular that is covered by recall Z-1131-2023 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.
