Food, drugs, devices › Megadyne Medical Products, Inc.
Device recall: Hand Control 12FR Suction Coagulator with 10 ft cord and holster, Sterile, Disposable, Model Number 0043-25, packaged Ty
FDA enforcement event 67641 is a device recall by Megadyne Medical Products, Inc. of Draper, UT, initiated 27 Feb 2014 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 91% of the 1,176 device enforcement events initiated in 2014 carry the same class.
Status: Terminated, terminated 9 Jul 2014. Initiation: voluntary: firm initiated. Megadyne Medical Products, Inc. has 8 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Megadyne Medical Products, Inc., Draper, UT.
Reason for recall
"Megadyne Medical Products, Inc. is voluntarily recalling Hand Control 12Fr Suction Coagulator with 10ft cord and 132405 Holster, Sterile, Disposable, Lot 132405 due to the potential for a small number of these suction coagulators to self-activate immediately on connection to the electrosurgical generator and to remain activated until it is disconnected."
Distribution
"USA including FL, MN, LA, NJ, NM, PA, TX and Internationally to Canada."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1151-2014 | Hand Control 12FR Suction Coagulator with 10 ft cord and holster, Sterile, Disposable, Model Number 0043-25, packaged Tyvek¿ polyester peel pouch, 25 pouches per box. This device is intended to conduct monopolar electrosurgical energy from an electrosurgical generator (ESU) to target tissue during ENT and general… | 494 | Class II | Terminated | 19 Mar 2014 |
Context
Other enforcement events for Megadyne Medical Products, Inc.
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 17 Jun 2024 | Brand Name: MEGADYNE" MEGA 2000" Patient Return Electrode Product Name: MEGADYNE" MEGA 2000" Patient Return Electrode Mo | Device | Class I | 3 |
| 8 May 2024 | MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patients weighing (0.8lb-50 | Device | Class I | 1 |
| 8 Dec 2023 | Product Code 0845, MEGADYNE MEGA SOFT Universal Patient Return Electrode, Reusable Patient Return Electrode | Device | Class I | 4 |
| 15 Jun 2023 | MEGADYNE Suction Coagulators, Product Code 004125 (Suction Coagulator, Handswitching, 10 Fr, 6 inch (15.24cm)), Product | Device | Class II | 1 |
| 1 Jun 2023 | MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery | Device | Class I | 8 |
| 15 May 2018 | MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715 | Device | Class II | 1 |
| 7 Aug 2013 | E-Z Clean¿ Disposable Laparoscopic Electrode Model Number 0100L and 0100LS. Expiration dates of 05/2018 to 07/2018. Ster | Device | Class II | 1 |
All 8 events for Megadyne Medical Products, Inc.
Questions and answers
Why was this device recalled?
FDA's record gives the reason for recall as: "Megadyne Medical Products, Inc. is voluntarily recalling Hand Control 12Fr Suction Coagulator with 10ft cord and 132405 Holster, Sterile, Disposable, Lot 132405 due to the potential for a small number of these suction coagulators to self-activate immediately on connection to the electrosurgical generator and to remain activated until it is disconnected."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "USA including FL, MN, LA, NJ, NM, PA, TX and Internationally to Canada."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 9 Jul 2014. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.