Data Foundry

Medical device recalls 2014

XiO RPT System The XiO RTP System is used to create treatment plans… — Class II medical device recall Z-1197-2014

Terminated recall by Elekta, Inc., reported 2014-03-19, distributed in AK, AL, AZ, CA, CO, CT, DC, DE…. Dose and Monitor Unit values are not computed correctly when Elekta Motorized Wedges are used with Dynamic Con

Recall numberZ-1197-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmElekta, Inc., Atlanta, GA, United States
Recall initiated2014-02-17
Classified2014-03-13
Reported by FDA2014-03-19
Terminated2015-07-21
DistributedAK, AL, AZ, CA, CO, CT, DC, DE, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NV, NY, OH, OK, PA, PR, RI, SC, TN, TX, VA, WA, WI, WV, WY
Countries outside the USAR, AT, AU, BB, BM, BR, BS, CA, CL, CN, CR, CW, CY, CZ, DE, DZ, EE, EG, ES, FI, FR, GB, GR, GT, HK, ID, IE, IL, IN, IQ, IT, JO, JP, KR, KW, MT, MX, MY, NG, NL, NZ, PE, PH, PK, PL, PT, RO, RS, RU, SG, SI, TH, TR, TW, UA, UY, VE, VN
Quantity1,776

Product

XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam radiation therapy or brachytherapy has been prescribed. The system will calculate and display, both on screen and in hard-copy, either two or three dimensional radiation dose distributions within a patient for a given treatment.

Reason for recall

Dose and Monitor Unit values are not computed correctly when Elekta Motorized Wedges are used with Dynamic Conformal arcs.

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-1197-2014. 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.