Achilles Insight Bone Sonometer
Reported: October 16, 2019 Initiated: September 3, 2019 #Z-0112-2020
Product Description
Achilles Insight Bone Sonometer
Reason for Recall
Certain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective earth connection.
Details
- Recalling Firm
- GE Healthcare, LLC
- Units Affected
- 599 devices
- Distribution
- Nationwide distribution to AZ, GA, MT, NC, NJ, NY, OH, WI. International distribution to Australia, Bahrain, Bangladesh, Brazil, Cambodia, Chile, China, Colombia, Cyprus, Hong Kong, India, Iraq, Ireland, Italy, Kuwait, Lebanon, Malaysia, Mauritius, Mexico, MEXICO, Myanmar, Nepal, Oman, Panama, Peru, Philippines, Saudi Arabia, Singapore, Sri Lanka, Switzerland, Taiwan, Thailand, United Arab Emirates, United Kingdom, Uruguay, Vietnam
- Location
- Waukesha, WI
Frequently Asked Questions
What product was recalled? ▼
Achilles Insight Bone Sonometer. Recalled by GE Healthcare, LLC. Units affected: 599 devices.
Why was this product recalled? ▼
Certain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective earth connection.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 16, 2019. Severity: Moderate. Recall number: Z-0112-2020.
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