Recall Register

Medical Action Industries, Inc. 306: FDA recalls

FDA enforcement reports name Medical Action Industries, Inc. 306 as the recalling firm in 15 events. The events have 25 product records. The recalls started from 2019 to 2026. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

15 events, newest first.

FDA enforcement events of Medical Action Industries, Inc. 306
InitiatedProduct (first record)TypeClassRecordsStatus
23 Jul 2026Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampulesDeviceClass I2Ongoing
23 Jul 2026Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B; Blood Culture Collection Kit, REF: 81834C. All containing BD ChloraPrep Clear - 1 mL ApplicatorsDeviceClass II1Ongoing
21 May 2026Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791DeviceClass II1Ongoing
13 May 2026Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle ManifoldsDeviceClass I1Ongoing
17 Mar 2026Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/CaseDeviceClass I1Ongoing
11 Jun 2024Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75 each/case), 6106 (250 each/case), 6141 (250 each/case), 6203 (40 each/case), 6805 (50 each/case), 6805-1 (175 each/case), 6810 (50 each/case), 6810-1 (350 each/case), 6830 (8 rolls/case), and 6860 (8…DeviceClass II1Ongoing
15 Jan 2024IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.DeviceClass II1Ongoing
4 Nov 2022Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kitDeviceClass II1Terminated
12 Oct 2022Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc. IV Start Kit, REF #78019 (on kit label), sterile. Kit components are the Port Access Kit.DeviceClass II1Terminated
12 Oct 2022Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.DeviceClass II1Terminated
15 Sep 2022B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)DeviceClass II1Terminated
8 Sep 2021Kit: Central Line Dres Change 20/CsDeviceClass II1Terminated
11 May 2021Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220DeviceClass II5Terminated
9 Apr 2021Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420DeviceClass I6Terminated
2 Dec 2019Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit, REF 77070B ***DIALYSIS*** Clear Sequence Change Kit, REF 77068B ***PEDS CVC*** Clear Sequence Change Kit, REF 77190B ***PICC*** Clear Sequence Change Kit, REF 77069B Adult Central Line Dressing Change…DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Medical Action Industries, Inc. 306: events for each product type
TypeEvents
Device15
Medical Action Industries, Inc. 306: events in each class
ClassEvents
Class II11
Class I4
Share of the events of the firm in Class I
27%
Share of all events on the register in Class I
18%
Events with the status Ongoing
7

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Medical Action Industries, Inc. 306, by the year that the recall started. The largest year is 2026, with 5 events.

Official channels

Cite this page

Recall Register. Medical Action Industries, Inc. 306: FDA recalls. https://recallregister.com/firm/medical-action-industries-inc-306/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
NC

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Medical Action Industries, Inc. 306 have?
Class II: 11 events. Class I: 4 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Medical Action Industries, Inc. 306?
FDA event 99613, which the firm started on 23 Jul 2026. The first product in the record is: Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
How many FDA recalls of Medical Action Industries, Inc. 306 have the status Ongoing?
7 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.