Medical Action Industries, Inc. 306 recalls

Medical Action Industries, Inc. 306 has 22 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 12 Aug 2026. 5 are still ongoing. 3 were reported in the last 12 months. The most frequent reason is packaging defects.

Total recalls22since 2020

Last 12 months3reported

Class I836% of total

Ongoing5latest 12 Aug 2026

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 1 0 0Jul 2 0

Severity split

Class I 8 36%Class II 14 64%Class III 0 0%

Why medical action industries, inc. 306 is recalled

Product types

By year

2026314%
202429%
2022418%
20211255%
202015%

Ongoing medical action industries, inc. 306 recalls

5 active

Reported	Class	Recall	Company	Reason	Where
12 Aug 2026Device	CLASS II	Medical Action Industries Dialysis Change Tray Clear Sequence recalled	Medical Action Industries, Inc. 306	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS I	Pack Angiography Ncmc 3/Cs Banner recalled by Medical Action Industries	Medical Action Industries, Inc. 306	Particulate Matter	AZ, CO
13 May 2026Device	CLASS I	Medical Action Industries Inc. Pack Cath BHH recalled	Medical Action Industries, Inc. 306	Sterility	AZ
18 Sep 2024Device	CLASS II	Foam Protective recalled by Medical Action Industries	Medical Action Industries, Inc. 306	Other	Nationwide
3 Apr 2024Device	CLASS II	IV Start Kit, containing 1 Saline Syringe recalled	Medical Action Industries, Inc. 306	Sterility	Nationwide

All medical action industries, inc. 306 recalls, newest first

22 total

Reported	Class	Recall	Company	Reason	Where
12 Aug 2026Device	CLASS II	Medical Action Industries Dialysis Change Tray Clear Sequence recalled	Medical Action Industries, Inc. 306	Packaging Defects	Nationwide
5 Aug 2026Device	CLASS I	Pack Angiography Ncmc 3/Cs Banner recalled by Medical Action Industries	Medical Action Industries, Inc. 306	Particulate Matter	AZ, CO
13 May 2026Device	CLASS I	Medical Action Industries Inc. Pack Cath BHH recalled	Medical Action Industries, Inc. 306	Sterility	AZ
18 Sep 2024Device	CLASS II	Foam Protective recalled by Medical Action Industries	Medical Action Industries, Inc. 306	Other	Nationwide
3 Apr 2024Device	CLASS II	IV Start Kit, containing 1 Saline Syringe recalled	Medical Action Industries, Inc. 306	Sterility	Nationwide
28 Dec 2022Device	CLASS II	Medical Action Industries INC. Port a Cath Kit recalled	Medical Action Industries, Inc. 306	Other	Nationwide
28 Dec 2022Device	CLASS II	Medical Action Industries Inc. Disposable Instrument Pack recalled	Medical Action Industries, Inc. 306	Sterility	8 states
14 Dec 2022Device	CLASS II	Medical Action Industries Inc. Port Access Kit recalled	Medical Action Industries, Inc. 306	Labeling Errors	MN
30 Nov 2022Device	CLASS II	B. Braun Caresite Port Access Kit w/Tegaderm recalled	Medical Action Industries, Inc. 306	Labeling Errors	Nationwide
27 Oct 2021Device	CLASS II	Kit: Central Line Dres Change 20/Cs recalled	Medical Action Industries, Inc. 306	Other	MI

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.