# FDA recall Z-2995-2020

> **GE Healthcare, LLC** · Class II · device recall initiated 2020-08-14.

## Product

NM 830  Model # H3910AC

## Reason for recall

Rotor bearing screws were found loose on  detector.

## Distribution

USA :  AR  CT  FL  GA  IL  KS  KY  LA  MA  MD  MI  MN  MO  NE  NJ  NV  NY  OH  OK  RI  SC  TN  TX  VA  VT  WA  WI          OUS:  ARGENTINA  AUSTRIA  BELGIUM  BRAZIL  Canada  CHINA  FRANCE  GERMANY  GREECE  INDIA  ISRAEL  ITALY  JAPAN  Korea (Republic of)  NETHERLANDS  NORWAY  PANAMA  POLAND  PORTUGAL  Russia  SPAIN  SWEDEN  SWITZERLAND  TAIWAN  THAILAND  TURKEY  UNITED KINGDOM  VIETNAM

## Key facts

- **Recall number:** Z-2995-2020
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-08-14
- **Report date:** 2020-09-30
- **Termination date:** 2021-05-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2995-2020

## Citation

> AI Analytics. FDA recall Z-2995-2020. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2995-2020. Source: US FDA. Licensed CC0.

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