HexaPOD evo RT Couchtop — Class II medical device recall Z-1514-2014
Terminated recall by Elekta, Inc., reported 2014-05-07, distributed in AZ, CA, CT, DC, FL, GA, HI, IL…. If screws are not properly tightened with a torque wrench they may become loose over time.
| Recall number | Z-1514-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elekta, Inc., Atlanta, GA, United States |
| Recall initiated | 2014-04-17 |
| Classified | 2014-04-25 |
| Reported by FDA | 2014-05-07 |
| Terminated | 2015-01-29 |
| Distributed | AZ, CA, CT, DC, FL, GA, HI, IL, KY, MA, MD, MI, MO, MS, NC, ND, NH, NJ, NY, OH, OK, OR, PA, SC, TX, VA, WA, WI, WY |
| Countries outside the US | AT, AU, BE, BR, CA, CH, CN, CO, CZ, DE, DK, DZ, FI, FR, GB, GR, HK, IL, IN, IT, JP, KR, MX, NL, NZ, PE, PL, PT, RU, SA, SE, TH, TR, TW |
| Quantity | 266 |
| Serial numbers | 29677, 2969, 2971, 2972, 2973, 2974, 2975, 2976, 2978, 2979, 2980, 2981, 2982, 2984, 2985, 2986, 2987, 2988, 2989, 2990, 2991, 2992, 2993, 2994, 2995 and 271 more |
Product
HexaPOD evo RT Couchtop. To support and aid in positioning a patient during radiation therapy.
Reason for recall
If screws are not properly tightened with a torque wrench they may become loose over time.
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-1514-2014. 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.