Civco Belly Board MRI — Class II medical device recall Z-0803-2014
Terminated recall by Civco Medical Instruments Inc, reported 2014-01-29, distributed nationwide. Scales adhered to the product may be misaligned from the zero reference such that one side will not match the
| Recall number | Z-0803-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Civco Medical Instruments Inc, Kalona, IA, United States |
| Recall initiated | 2013-10-25 |
| Classified | 2014-01-21 |
| Reported by FDA | 2014-01-29 |
| Terminated | 2017-02-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, BR, CA, CL, CZ, DE, ES, FR, IL, IQ, IT, JP, KR, MY, SA, SI, TR |
| Quantity | 2 belly |
| Lot numbers | M550150, M551490 |
| Model numbers | 126000 |
Product
Civco Belly Board MRI, Reusable non-sterile glass fiber belly board with cushion, REF 126000, packaged 1 per box. Product Usage: This device is intended to reduce the irradiated small bowel volume of gynecological patients undergoing treatment in the pelvic region.
Reason for recall
Scales adhered to the product may be misaligned from the zero reference such that one side will not match the other.
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-0803-2014. 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.