Reported Apr 20, 2022 · Ongoing
20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
Abbott Vascular
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Abbott Vascular · 26531 Ynez Rd · Temecula, CA · 92591-4630
Is this the product you have?
- 20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
- Lot codes and dates
- Part Numbers1000184
- Device Identifier-GTIN08717648013591
- Lot Numbers
6030967860320071603371626031133660320899603371666031133860331726603113376031133960331727603175396031591460334491603182096031753560334492
- Amount recalled
- 17 lots
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Due to an increase in complaint trend for leaks and intermittent/loose connections.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Abbott Vascular recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.