# Caerus Corp. dba Orthocor Medical – FDA 483, Feb 27, 2026

Source: https://www.keypedia.com/records/483/caerus-corp-dba-orthocor-medical/da68a467-59eb-421c-b61e-51c84b1000b1

> FDA 483 for Caerus Corp. dba Orthocor Medical on February 27, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Caerus Corp. dba Orthocor Medical
- Inspection Date: 2026-02-27
- Product Type: device
- Office Name: Minneapolis District Office
- Summary: Caerus Corp dba OrthoCor Medical, a medical device manufacturer in Blaine, MN, received a Form 483 for significant deficiencies in their quality system. The inspection revealed inadequate corrective and preventive actions (CAPA) that failed to address recurring product issues like charging port failures and incorrect activation for approximately four years. Additionally, the firm's risk management processes, specifically Failure Mode and Effects Analysis (FMEA) documents, did not adequately capture and assess hazard/failure modes reported through customer complaints.

## Related Documents

- [483 - 2022-11-22](https://www.keypedia.com/records/483/caerus-corp-dba-orthocor-medical/24cef1ee-6b39-4291-bc88-1e137d5a9f22) — date: November 22, 2022
- [483 - 2019-04-24](https://www.keypedia.com/records/483/caerus-corp-dba-orthocor-medical/b1d0f574-14ec-4959-9c67-ebb8a0f6b442) — date: April 24, 2019

## Related Officers

- [Benjamin W. Anderson](https://www.keypedia.com/people/benjamin-w-anderson/a3c0961c-6a83-4bd7-abb8-02c5c8dd3a35)

Company: https://www.keypedia.com/companies/caerus-corp-dba-orthocor-medical/5bbb3b68-b24e-42b4-b35d-5aae22299e2c

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d