GEO-MED ORTHO TOTAL JOINT TRACECART — Class II medical device recall Z-1692-2013
Terminated recall by DeRoyal Industries Inc, reported 2013-07-17, distributed nationwide. DeRoyal recalled kits that contained Stryker togas which were recalled for a potential problem with sterilizat
| Recall number | Z-1692-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DeRoyal Industries Inc, Powell, TN, United States |
| Recall initiated | 2013-05-30 |
| Classified | 2013-07-11 |
| Reported by FDA | 2013-07-17 |
| Terminated | 2013-07-12 |
| Distributed | Nationwide (US) |
| Quantity | 87 units |
| Serial numbers | 25405311, 25405485, 25556398, 25866038, 25920479, 25969803, 26040887, 26092011, 26092089, 26109451, 26198457, 26262324, 26330892, 26394079, 26568438, 26637085, 26695568, 26938574, 26942371, 26946478, 27751648, 27860730, 27905871, 27915366 |
| Model numbers | 53-1831.07 |
Product
GEO-MED ORTHO TOTAL JOINT TRACECART(R), REF 53-1831.07, Rx Only, NON-STERILE Product Usage: general surgical
Reason for recall
DeRoyal recalled kits that contained Stryker togas which were recalled for a potential problem with sterilization.
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-1692-2013. 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.