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Terumo BCT recalls

Terumo BCT has 4 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 22 Nov 2017. The most frequent reason is sterility.

Total recalls4since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 22 Nov 2017

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 4 100%Class III 0 0%

Why terumo bct is recalled

Sterility375%
Labeling Errors125%

Product types

Other Medical Devices4100%

By year

2017375%
2016125%

All terumo bct recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
22 Nov 2017Device	CLASS II	Harvest(R) Terumobct, BMAC2-120-01Bone Marrow Procedure Pack recalled	Terumo BCT	Sterility	7 states
22 Nov 2017Device	CLASS II	Harvest(R) Terumobct, Bmac-30-07 Bone Marrow Procedure Pack recalled	Terumo BCT	Sterility	7 states
15 Nov 2017Device	CLASS II	Harvest Terumobct, Gcp-10 Graft Delivery Pack recalled	Terumo BCT	Sterility	Nationwide
7 Dec 2016Device	CLASS II	Adiprep Adipose Transfer System recalled by Terumo BCT	Terumo BCT	Labeling Errors	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.