1 — Class II medical device recall Z-0526-2022
Ongoing recall by NRT X-RAY A/S, reported 2022-02-02, distributed in IA, KY, LA, MA, NC, NY, OH, SC…. Friction rubber block in the clamping mechanism was missing in the Footrest. It may slip down along the patien
| Recall number | Z-0526-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | NRT X-RAY A/S, Hasselager, Denmark |
| Recall initiated | 2022-01-21 |
| Classified | 2022-01-25 |
| Reported by FDA | 2022-02-02 |
| Distributed | IA, KY, LA, MA, NC, NY, OH, SC, WA, WV |
| Countries outside the US | CH, CZ, DE, DK, NL, SE |
| Quantity | 72 units |
| UPC / GTIN / UDI-DI | 00903282000006, 00903282000020, 00903282000044, 00903282000051, 00903282000068, 00903282000075, 00903283000005, 00903283000012, 05713464000336, 05713464000381 |
| Serial numbers | 903282000001, 903282000002, 903282000004, 9032820000070, 903282000046, 903282000057, 903282000075, 903283000001, 903283000012, 903283000028 |
| Model numbers | 03282000, 03283000 |
Product
1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices)
Reason for recall
Friction rubber block in the clamping mechanism was missing in the Footrest. It may slip down along the patient table while in use with a patient. This accessory is designed to use with Intelli-C, Right and Intelli-C, Left.
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-0526-2022. 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.