Medical Action Industries Inc. 306 recalls

Medical Action Industries Inc. 306 has 26 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 14 Oct 2026. 9 are still ongoing. 7 were reported in the last 12 months. The most frequent reason is packaging defects.

Total recalls26since 2020

Last 12 months7reported

Class I1038% of total

Ongoing9latest 14 Oct 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 1May 0 0 2Aug 3 1

Severity split

Class I 10 38%Class II 15 58%Class III 1 4%

Why medical action industries inc. 306 is recalled

Product types

By year

2026727%
202428%
2022415%
20211246%
202014%

Ongoing medical action industries inc. 306 recalls

9 active

Reported	Class	Recall	Company	Reason	Where
14 Oct 2026Device	CLASS III	Kit: Urinary Clean Catch 20/cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Device Malfunction	CA
23 Sep 2026Device	CLASS II	Blood Culture Collection Venipuncture Kit 20/Cs recalled	Medical Action Industries Inc. 306	Sterility	Nationwide
16 Sep 2026Device	CLASS I	Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS I	Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
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

All medical action industries inc. 306 recalls, newest first

26 total

Reported	Class	Recall	Company	Reason	Where
14 Oct 2026Device	CLASS III	Kit: Urinary Clean Catch 20/cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Device Malfunction	CA
23 Sep 2026Device	CLASS II	Blood Culture Collection Venipuncture Kit 20/Cs recalled	Medical Action Industries Inc. 306	Sterility	Nationwide
16 Sep 2026Device	CLASS I	Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS I	Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
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	Other	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	Other	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	Packaging Defects	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
30 Jun 2021Device	CLASS II	Medical Action Industries INC. recalled	Medical Action Industries Inc. 306	Foreign Material	Nationwide
30 Jun 2021Device	CLASS II	Medical Action Industries INC., General Purpose Instrument Tray recalled	Medical Action Industries Inc. 306	Foreign Material	Nationwide
30 Jun 2021Device	CLASS II	Medical Action Industries INC. recalled	Medical Action Industries Inc. 306	Foreign Material	Nationwide
30 Jun 2021Device	CLASS II	Medical Action Industries INC., Minor Procedure Tray recalled	Medical Action Industries Inc. 306	Foreign Material	Nationwide
30 Jun 2021Device	CLASS II	novaplus, General Purpose Kit recalled by Medical Action Industries	Medical Action Industries Inc. 306	Foreign Material	Nationwide
19 May 2021Device	CLASS I	Kit: Blood Culture MAI Kit recalled by Medical Action Industries	Medical Action Industries Inc. 306	Packaging Defects	Nationwide
19 May 2021Device	CLASS I	Kit: Injection Review MAI Kit recalled by Medical Action Industries	Medical Action Industries Inc. 306	Packaging Defects	Nationwide
19 May 2021Device	CLASS I	Kit: Midline Insertion DA recalled by Medical Action Industries	Medical Action Industries Inc. 306	Packaging Defects	Nationwide
19 May 2021Device	CLASS I	Kit: Blood Culture recalled by Medical Action Industries	Medical Action Industries Inc. 306	Packaging Defects	Nationwide
19 May 2021Device	CLASS I	Kit: CentralLineDresChangeClrSeq MAI Kit recalled	Medical Action Industries Inc. 306	Packaging Defects	Nationwide
19 May 2021Device	CLASS I	Kit: LVAD Dres Chg recalled by Medical Action Industries	Medical Action Industries Inc. 306	Packaging Defects	Nationwide
15 Jan 2020Device	CLASS II	Medical convenience trays and kits, labeled as recalled	Medical Action Industries Inc. 306	Other	21 states

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.