ANTHEM 71422844Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00885556531471), received between Aug 21, 2019 and Mar 24, 2020 — classified as 3 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

1 other recall cover devices cleared under the same FDA submission (K142807, K230653); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMar 24, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A TRANSFUSION (PRC) WAS PERFORMED SINCE PATIENT PRESENTED ANEMIA.

  Patient problems: Anemia

  MAUDE report 9875394 ↗
• InjuryJan 13, 2020Physical Resistance/Sticking; Physical Resistance/Sticking

  (B)(6). IT WAS REPORTED A STIFF RIGHT KNEE SO A PROCEDURE WAS PERFORMED.

  Patient problems: Injury

  MAUDE report 9580092 ↗
• InjuryAug 21, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT A PERCUTANEOUS INFERIOR VENA CAVA RETRIEVABLE FILTER IMPLANTATION WAS PERFORMED UNDER LOCAL ANESTHESIA DUE TO DEEP VENOUS THROMBOSIS.

  Patient problems: Injury

  MAUDE report 8919246 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K142807, K230653. One submission often covers many models, so check the product and lot details in each record.

• Z-2621-2023 · Aug 31, 2023 · Open, Classified
  smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT, SIZE 5N, LEFT, NARROW, REF 71421265; knee joint