DeRoyal TRACECART POSTEROR LUMBAR FUSION TRACECART — Class II medical device recall Z-0707-2023
Ongoing recall by DeRoyal Industries Inc, reported 2022-12-21, distributed in AL, AZ, CT, FL, GA, IL, IN, KS…. XXX
| Recall number | Z-0707-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | DeRoyal Industries Inc, Powell, TN, United States |
| Recall initiated | 2022-11-03 |
| Classified | 2022-12-15 |
| Reported by FDA | 2022-12-21 |
| Distributed | AL, AZ, CT, FL, GA, IL, IN, KS, LA, MA, MI, MN, MO, MS, NC, NJ, NY, OH, PA, TN, TX, VA, WI |
| Quantity | 336 kits |
| Lot numbers | 56169083, 56357092, 56481018, 56538205, 56873265, 56895966, 56942611, 57088584, 57088592, 57180516, 57270562, 57313163, 57313171, 57492608, 57646152, 57681329, 57717598, 57788708, 57889681, 57928563, 57960070, 58003845, 58032523 |
| Model numbers | 53-1961.02 |
| Expiration dates | 2023-09-01, 2023-12-01, 2024-03-01, 2024-04-01 |
Product
DeRoyal TRACECART POSTEROR LUMBAR FUSION TRACECART, REF 53-1961.02
Reason for recall
XXX
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-0707-2023. 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.