PlainRecalls

Medical Action Industries, Inc. 306

Compiled from official public sources by the editorial team.

20 recalls on record · Latest: May 13, 2026

Medical Action Industries, Inc. 306 Recall Insight

Medical Action Industries, Inc. 306 appears on 20 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.020% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated May 13, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 20 entries, severity tagging shows 7 critical, 13 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 20 of 20 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (20). The date window on this page runs from Jan 15, 2020 to May 13, 2026.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Critical May 13, 2026

Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

FDA Devices Moderate Sep 18, 2024

Foam 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), …

FDA Devices Moderate Apr 3, 2024

IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.

FDA Devices Moderate Dec 28, 2022

Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.

FDA Devices Moderate Dec 28, 2022

Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit

FDA Devices Moderate Dec 14, 2022

Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc. IV Start Kit, REF #78019 (o…

FDA Devices Moderate Nov 30, 2022

B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)

FDA Devices Moderate Oct 27, 2021

Kit: Central Line Dres Change 20/Cs

FDA Devices Moderate Jun 30, 2021

novaplus, General Purpose Kit, Cat. No. 56603

FDA Devices Moderate Jun 30, 2021

Medical Action INDUSTRIES INC., Minor Procedure Tray, REF 61214

FDA Devices Moderate Jun 30, 2021

Medical Action INDUSTRIES INC., Disposable Instrument Pack Curved Hemostat, REF 56224

FDA Devices Moderate Jun 30, 2021

Medical Action INDUSTRIES INC., General Purpose Instrument Tray, REF 61209

FDA Devices Moderate Jun 30, 2021

Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220

FDA Devices Critical May 19, 2021

Kit: LVAD Dres Chg. MAI Kit Part Number: 79544B

FDA Devices Critical May 19, 2021

Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420

FDA Devices Critical May 19, 2021

Kit: Blood Culture. MAI Kit Part Number: 80315D

FDA Devices Critical May 19, 2021

Kit: Midline Insertion DA. MAI Kit Part Number: 77981B

FDA Devices Critical May 19, 2021

Kit: Injection REVIEW MAI Kit Part Number: 74736

FDA Devices Critical May 19, 2021

Kit: Blood Culture MAI Kit Part Number: 80076

FDA Devices Moderate Jan 15, 2020

Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit, REF 77070B ***DIALYSIS*** …

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.