Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2827-2020 — 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

U.S. FDA — Device Enforcement · Switzerland · 2020-07-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2827-2020
Date of alert: 2020-07-22
Country / jurisdiction: Switzerland
Risk level: Class II
Risk type: recall
Brand: Smith & Nephew Orthopaedics AG
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 75102205

Reported risk: Multiple lots being recalled due to a product design issue

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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