PlainRecalls

Megadyne Medical Products, Inc.

Compiled from official public sources by the editorial team.

20 recalls on record · Latest: Jul 10, 2024

Megadyne Medical Products, Inc. Recall Insight

Megadyne Medical Products, Inc. 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 Jul 10, 2024, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 20 entries, severity tagging shows 16 critical, 4 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 19 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 Sep 4, 2013 to Jul 10, 2024.

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 Jul 10, 2024

Brand Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Model/Catal…

FDA Devices Critical Jul 10, 2024

Brand Name: MEGADYNE" MEGA 2000" Patient Return Electrode Product Name: MEGADYNE" MEGA 2000" Patient Return Electrode Model/Catalog Number: 0800 S…

FDA Devices Critical Jul 10, 2024

Brand Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode M…

FDA Devices Critical Jun 12, 2024

MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patients weighing (0.8lb-50lb), (350g-22.7Kg), 66cm Long…

FDA Devices Critical Jan 3, 2024

Product Code 0848, MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Dual Plus

FDA Devices Critical Jan 3, 2024

Product Code 0847, MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Plus

FDA Devices Critical Jan 3, 2024

Product Code 0846, MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Dual Cord

FDA Devices Critical Jan 3, 2024

Product Code 0845, MEGADYNE MEGA SOFT Universal Patient Return Electrode, Reusable Patient Return Electrode

FDA Devices Moderate Aug 9, 2023

MEGADYNE Suction Coagulators, Product Code 004125 (Suction Coagulator, Handswitching, 10 Fr, 6 inch (15.24cm)), Product Code 004225 (Suction Coagulat…

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during electrosurgery

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during electrosurgery

FDA Devices Moderate Aug 22, 2018

MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715

FDA Devices Moderate Mar 19, 2014

Hand Control 12FR Suction Coagulator with 10 ft cord and holster, Sterile, Disposable, Model Number 0043-25, packaged Tyvek¿ polyester peel pouch, 25…

FDA Devices Moderate Sep 4, 2013

E-Z Clean¿ Disposable Laparoscopic Electrode Model Number 0100L and 0100LS. Expiration dates of 05/2018 to 07/2018. Sterile. RX ONLY. This product …

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Megadyne Medical Products, Inc. with Zimmer Biomet, Inc. →

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.