Recalls · Brand

Orthosoft, Inc. dba Zimmer CAS recalls

Every recall we track for Orthosoft, Inc. dba Zimmer CAS — 1 in all, all from 2022 — plus the complaints and injury reports the public filed about them.

1recalls

Recalls per year, by danger level

1 recall since 2017.

All FDA recall records for Orthosoft, Inc. dba Zimmer CAS since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Orthosoft, Inc. dba Zimmer CAS, by danger level
Year	Lower risk	Total
2017	0	0
2018	0	0
2019	0	0
2020	0	0
2021	0	0
2022	1	1
2023	0	0
2024	0	0
2025	0	0
2026 (to date)	0	0

What to do if you have a recalled Orthosoft, Inc. dba Zimmer CAS product

Match the model, catalog or lot number on your device to the recall.
Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
Report problems to FDA MedWatch.

See this week’s new recalls.

All Orthosoft, Inc. dba Zimmer CAS recalls

1 shown

Lower riskMedical device
Orthosoft, Inc. dba Zimmer CAS recalls NavitrackER Kit A: Knee, Model Number 20-8000-000-07,
Zimmer CAS recalls NavitrackER Knee Kit A (Model 20-8000-000-07) due to potential infection from insufficient sterilization. Affected units sold with lot 110221A1 and UDI number (01)00889024304222.
Zimmer CASJan 7, 2022

Orthosoft, Inc. dba Zimmer CAS recall questions

How many recalls has Orthosoft, Inc. dba Zimmer CAS had?

1 recall from Orthosoft, Inc. dba Zimmer CAS are on record with U.S. safety agencies, from 2022.

What is the most recent Orthosoft, Inc. dba Zimmer CAS recall?

Orthosoft, Inc. dba Zimmer CAS recalls NavitrackER Kit A: Knee, Model Number 20-8000-000-07,, dated Jan 7, 2022. Every Orthosoft, Inc. dba Zimmer CAS recall is listed on this page, newest first.

What should I do if I have a recalled Orthosoft, Inc. dba Zimmer CAS product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new Orthosoft, Inc. dba Zimmer CAS recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.