Reported Oct 16, 2019 · Terminated
Achilles Express Bone Sonometer
GE Healthcare, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: GE Healthcare, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615
Is this the product you have?
- Achilles Express Bone Sonometer
- Lot codes and dates
- System ID
241 of 241 codes
ACE34924AWE11358ACE34606ACE34652ACE34651AWE11894AWE1196ACE34927ACE886HAWE10447AWE11047AWE11098AWE11304AWE11312AWE11317AWE11381AWE11285ACH+12937ACH+12932ACH+12939ACH+12935ACH+12942ACH+12936ACH+12943ACH+12938ACH+12945ACH+12940ACH+12947ACH+12952ACH+12948ACH+12871ACH+12933ACH+12872ACH+12931ACH+12290ACH+12955ACH+12975ACH+12978ACH+12983GAACH+12986279840128158672858452287698826934190002722584AACH10439ACH31114ACH10346ACH10364ACH10393828330086828330087828330097828330098828330115828330091828330099828330119828330117
- System ID
- Amount recalled
- 241 devices
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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