Integra recalls

Integra has 9 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 22 May 2019. The most frequent reason is potency & assay.

Total recalls9since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 22 May 2019

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 9 100%Class III 0 0%

Why integra is recalled

Product types

By year

2019444%
2013222%
2012333%

All integra recalls, newest first

9 total

Reported	Class	Recall	Company	Reason	Where
22 May 2019Device	CLASS II	Flowable Wound Matrix recalled by Integra	Integra	Potency & Assay	Nationwide
17 Apr 2019Device	CLASS II	bioBLOCK Resorbable subtaler Implant recalled by Integra	Integra	Temperature Abuse	Nationwide
17 Apr 2019Device	CLASS II	bioBLOCK Resorbable subtaler Implant recalled by Integra	Integra	Temperature Abuse	Nationwide
17 Apr 2019Device	CLASS II	bioBLOCK Resorbable subtaler Implant recalled by Integra	Integra	Temperature Abuse	Nationwide
6 Nov 2013Device	CLASS II	Intracranial Pressure and Pressure-Temperature Monitoring recalled	Integra	Sterility	Nationwide
4 Sep 2013Device	CLASS II	Leyla Ball Joint Clamp, also as included recalled by Integra	Integra	Potency & Assay	23 states
3 Oct 2012Device	CLASS II	The Mayfield¿ Horseshoe Gel Pads are used recalled by Integra	Integra	Foreign Material	Nationwide
3 Oct 2012Device	CLASS II	The Mayfield¿ Horseshoe Gel Pads are used recalled by Integra	Integra	Foreign Material	Nationwide
25 Jul 2012Device	CLASS II	Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments recalled	Integra	Potency & Assay	Nationwide

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.