Reported May 16, 2018 · Terminated
Retractor f/Sciatic Nerve Long; Part number: 03.100.014; UDI: 10886982070630
Synthes (USA) Products 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: Synthes (USA) Products LLC · 1301 Goshen Pkwy · West Chester, PA · 19380-5986
Is this the product you have?
- Retractor f/Sciatic Nerve Long
- Part number03.100.014
- UDI10886982070630
- Lot codes and dates
- Lot numbers
T104993T108115T114598T140566T140665T140670T140671T140673T141540T143687T144854T145585T145590T145932T146657T147929T148552T148553T149727T149728 T151369T151488T152808T152809T153884T155649T958061
- Lot numbers
- Amount recalled
- 196
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
There is a potential for microspores to form on the hollow handle of the Sciatic Nerve Retractor. The pores may increase in size, allowing fluid to enter the hollow handle.
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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