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Amd-Ritmed recalls

Amd-Ritmed has 3 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 14 Dec 2016. The most frequent reason is sterility.

Total recalls3since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 14 Dec 2016

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 amd-ritmed is recalled

Sterility3100%

Product types

Other Medical Devices3100%

By year

20163100%

All amd-ritmed recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
14 Dec 2016Device	CLASS II	Transparent Dressing - Window with label, 4 " x 4 3/4" recalled	Amd-Ritmed	Sterility	4 states
27 Jul 2016Device	CLASS II	Conforming Stretch Gauze Bandages, Sterile x 4/1 yds recalled	Amd-Ritmed	Sterility	CA, NY, TN
6 Apr 2016Device	CLASS II	IMCO Conforming Stretch Gauze Bandages, Yds/ x recalled by Amd Ritmed	Amd Ritmed	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.