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I-Flow recalls

I-Flow has 3 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 12 Jun 2013. The most frequent reason is device malfunction.

Total recalls3since 2012

Last 12 months0reported

Class I133% of total

Ongoing0latest 12 Jun 2013

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 1 33%Class II 2 67%Class III 0 0%

Why i-flow is recalled

Device Malfunction3100%

Product types

Heart & Vascular Devices267%
Surgical Instruments133%

By year

2013267%
2012133%

All i-flow recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
12 Jun 2013Device	CLASS II	ON-Q Pain Relief System, T-Block Needle/Catheter Kit recalled by I-Flow	I-Flow	Device Malfunction	Nationwide
12 Jun 2013Device	CLASS II	ON-Q Pain Relief System, T-Block Needle/Catheter Tray recalled by I-Flow	I-Flow	Device Malfunction	Nationwide
5 Sep 2012Device	CLASS I	On-q pump with Ondemand bolus button, On-q C-bloc with Ondemand recalled	I-Flow	Device Malfunction	CA

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.