Elekta Precise Treatment Table — Class II medical device recall Z-1238-2015
Terminated recall by Elekta, Inc., reported 2015-03-25, distributed nationwide. It is possible to position the Treatment Table with errors greater than 5mm and no inhibits are displayed, if
| Recall number | Z-1238-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elekta, Inc., Atlanta, GA, United States |
| Recall initiated | 2015-01-29 |
| Classified | 2015-03-19 |
| Reported by FDA | 2015-03-25 |
| Terminated | 2021-11-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, AU, BD, BE, BG, BH, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DK, DZ, EC, EG, ES, FI, FR, GR, HK, HN, HR, HU, ID, IE, IL, IN, IR, IT, JO, JP, KR, LB, LT, MA, MT, MX, MY, NG, NL, NO, NZ, PA, PE, PH, PK, PL, PT, RS, RU, SA, SE, SG, SI, SK, ZA |
| Serial numbers | 123318-330, 125807-880, 125883-899, 125902-917, 125920-949, 125952-963, 125966-1256453, 126158-170, 126174-208, 126212-230, 126232-261, 126269-281, 126293-309, 126338-126373, 126375-397, 126400-133999 |
Product
Elekta Precise Treatment Table
Reason for recall
It is possible to position the Treatment Table with errors greater than 5mm and no inhibits are displayed, if the positional sensors are not correctly installed during corrective maintenance. Clinical mistreatment may occur if a position error is not detected.
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-1238-2015. 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.