# FDA recall Z-0601-2020

> **CooperSurgical, Inc.** · Class II · device recall initiated 2019-10-16.

## Product

Quantam 2000 Electrosurgical Generator, Part number 909075-05.

## Reason for recall

Potential for the Quantum 2000 Electrosurgery Generator, part numbers 909075, 909075-05 and 909075-05W, to cease to either cut, coagulate, or blend during a procedure when the foot pedal is used for activation.

## Distribution

US: AL, AZ, CA, CO, FL, GA, HI, ID, IL, IN, LA,  MA, ME, Ml, MT, ND, NJ, NV, NY, OK, PA, SC, SD,  TN, TX, UT, VA, WA, & WV.  International: China, Indonesia, South Africa, & Tanzania.

## Key facts

- **Recall number:** Z-0601-2020
- **Recalling firm:** CooperSurgical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-16
- **Report date:** 2019-12-11
- **Termination date:** 2020-06-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Trumbull, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0601-2020

## Citation

> AI Analytics. FDA recall Z-0601-2020. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-0601-2020. Source: US FDA. Licensed CC0.

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