Advanced Orthogonal Percussion Adjusting Instrument Indicated for use… — Class II medical device recall Z-1809-2013
Terminated recall by Advanced Orthogonal Equipment, Incorporated, reported 2013-07-31, distributed nationwide. Unapproved medical device
| Recall number | Z-1809-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advanced Orthogonal Equipment, Incorporated, Saint Petersburg, FL, United States |
| Recall initiated | 2013-03-06 |
| Classified | 2013-07-25 |
| Reported by FDA | 2013-07-31 |
| Terminated | 2019-11-25 |
| Distributed | Nationwide (US) |
| Quantity | 54 |
| Reason classes | unapproved product |
| Serial numbers | 001, 0010, 002, 006, 007, 008, 009, 011, 014, 015, 016, 017, 018, 019, 020, 021, 022, 023, 024, 025, 026, 027, 028, 029, 030 and 27 more |
Product
Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra.
Reason for recall
Unapproved medical device
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1809-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.