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TissueTech recalls

TissueTech has 3 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 16 Dec 2020. The most frequent reason is sterility.

Total recalls3since 2020

Last 12 months0reported

Class I00% of total

Ongoing0latest 16 Dec 2020

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 3 100%Class III 0 0%

Why tissuetech is recalled

Sterility3100%

Product types

Other Medical Devices3100%

By year

20203100%

All tissuetech recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
16 Dec 2020Device	CLASS II	Prokera Slim, non-sterile recalled by TissueTech	TissueTech	Sterility	Nationwide
16 Dec 2020Device	CLASS II	Prokera, non-sterile recalled by TissueTech	TissueTech	Sterility	Nationwide
16 Dec 2020Device	CLASS II	Prokera Plus, non-sterile recalled by TissueTech	TissueTech	Sterility	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.