[Recalled] POLARSTEM COLLAR Reamer Guide, Catalog Number: 75102205, UPC Codes: 00885556535493 - Product Usage: Once the appropriate trial rasp size is in place, the adapter is removed and the calcar reamer guide (75102205) is positioned on
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | POLARSTEM COLLAR Reamer Guide, Catalog Number: 75102205, UPC Codes: 00885556535493 - Product Usage: Once the appropriate trial rasp size is in place, the adapter is removed and the calcar reamer guide (75102205) is positioned on the rasp. The calcar reamer (75102207 or 75102208) is placed over the r |
|---|---|
| Brand / manufacturer | Smith & Nephew Orthopaedics AG |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2827-2020 |
| Country of notice | Switzerland |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 22 July 2020 |
| EAN / barcode | 75102205 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Multiple lots being recalled due to a product design issue
This Class II recall concerns device products distributed in Switzerland and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.