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BioDerm recalls

BioDerm has 3 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 18 Jun 2014. The most frequent reason is sterility.

Total recalls3since 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 18 Jun 2014

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 bioderm is recalled

Sterility3100%

Product types

Heart & Vascular Devices267%
Other Medical Devices133%

By year

20143100%

All bioderm recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
18 Jun 2014Device	CLASS II	Liberty 0 External Male Catheter Specialty Type recalled by BioDerm	BioDerm	Sterility	Nationwide
18 Jun 2014Device	CLASS II	Safe n' Dry 21006 (Component: Skin-prep Protective wipes) recalled	BioDerm	Sterility	Nationwide
18 Jun 2014Device	CLASS II	Liberty Pouch Clean & Dry External Male Catheter Specialty recalled	BioDerm	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.