Reported Oct 24, 2012 · Terminated
"***Electric Systems Foot Control with Direction Only***Rx Only***" Product Usage: Cutting and shaping bone including…
The Anspach Effort, Inc.
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: The Anspach Effort, Inc. · 4500 Riverside Drive · Palm Beach Gardens, FL · 33410-4235
Is this the product you have?
- "***Electric Systems Foot Control with Direction Only***Rx Only***"
- Product UsageCutting and shaping bone including bones of the spine and cranium
- Lot codes and dates
- Serial Numbers
E28305271001E28305271002E28305271003E28305271004E2830527100E28305271006E28305271007E28305271008E2830521009E28305271010E29305270901E29305270902E29305270903E29305271101E29305271102E29305271103E29305271104E29305271105E29305271106E29305271107E29
- Serial Numbers
- Amount recalled
- 41 units
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
- Nationwide
Why it was recalled
The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot control/foot pedal due to the Foot Control Cable lacking the shield connection from the cable to the connector body.
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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