Reported Nov 27, 2013 · Terminated
Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
Aesculap, 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: Aesculap, Inc. · 3773 Corporate Pkwy · Center Valley, PA · 18034-8217
Is this the product you have?
- Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
- Lot codes and dates
- model no. ME020R
- Amount recalled
- 30
Where it was sold
Why it was recalled
The trial insertion instrument may disassemble during use due to a potentially weak weld on then trial inserter shaft block area located near the thumb wheel.
This product could cause temporary or reversible health problems — stop using it.
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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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