Accusorb MRI MAC7030 Product Usage: Radio frequency shielding… — Class II medical device recall Z-0673-2016
Terminated recall by MWT Materials, Inc., reported 2016-01-27, distributed nationwide. When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
| Recall number | Z-0673-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MWT Materials, Inc., Passaic, NJ, United States |
| Recall initiated | 2014-10-06 |
| Classified | 2016-01-20 |
| Reported by FDA | 2016-01-27 |
| Terminated | 2021-07-13 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
| Reason classes | device malfunction |
Product
Accusorb MRI MAC7030 Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
Reason for recall
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.
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-0673-2016. 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.