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Impact Instrumentation recalls

Impact Instrumentation has 2 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 26 Sep 2012. The most frequent reason is packaging defects.

Total recalls2since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 26 Sep 2012

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 0 0%Class II 0 0%Class III 2 100%

Why impact instrumentation is recalled

Packaging Defects150%
Device Malfunction150%

Product types

Other Medical Devices150%
CPAP & Ventilators150%

By year

20122100%

All impact instrumentation recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
26 Sep 2012Device	CLASS III	Model 324JL On-Board Suction System Intended use: On-board suction recalled	Impact Instrumentation	Packaging Defects	Nationwide
15 Aug 2012Device	CLASS III	Model 731 EMV+ Uni-Vent, Impact Instrumentation Inc., 27 Fairfield recalled	Impact Instrumentation	Device Malfunction	IL

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.