Abbott Vascular INDEFLATOR Plus 30 Recall: Leaks and Loose Connections

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Contact the company & request your remedy

Recalling firmAbbott Vascular26531 Ynez Rd, N/A · Temecula, CA 92591-4630

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Abbott Vascular is recalling INDEFLATOR Plus 30 devices due to reported leaks and intermittent/loose connections. This could lead to improper function of the device, potentially causing safety issues for users.

Why it’s dangerous

The device may develop leaks or loose connections due to manufacturing issues, which could cause improper function. This might lead to incorrect medical procedures or device failure during use.

Who’s affected

Users of the INDEFLATOR Plus 30 device with specific part numbers and lot numbers from March 2019 are affected. Medical professionals using this device for vascular procedures are at higher risk.

How to tell if you have this one

Check for part numbers 1000183 and lot numbers 60316775, 60322179, 60328352, 60322176, 60326322, or 60337153. The device was sold starting March 1, 2019.

Brand
Abbott Vascular
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Details
Verify your INDEFLATOR Plus 30 has part number 1000183 and one of the listed lot numbers from March 2019.

✎ GovInfoNow

Questions people ask

Why is this device being recalled?

Abbott Vascular recalls the INDEFLATOR Plus 30 due to an increase in complaints about leaks and intermittent/loose connections.

What should I do if I have this device?

Check if your device has part number 1000183 and one of the listed lot numbers from March 2019. If so, contact Abbott Vascular for further instructions.

Is there a fix for this issue?

The recall record does not specify a remedy or fix for the device issue.

Take action

Contact Abbott Vascular

We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0924-2022 — Abbott Vascular Abbott Vascular

Hello,

I own a Abbott Vascular that is covered by recall Z-0924-2022 from Abbott 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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Where this comes from

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-0924-2022 (March 11, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0924-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

Abbott Vascular recalls INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)

Lower-risk recall