The I-Cart is used to store — Class II medical device recall Z-1240-2015
Terminated recall by Richard Wolf Medical Instruments Corp., reported 2015-03-11, distributed nationwide. The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke and
| Recall number | Z-1240-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Richard Wolf Medical Instruments Corp., Vernon Hills, IL, United States |
| Recall initiated | 2014-12-10 |
| Classified | 2015-03-03 |
| Reported by FDA | 2015-03-11 |
| Terminated | 2017-07-31 |
| Distributed | Nationwide (US) |
| Quantity | 83 carts |
| Reason classes | packaging, device malfunction |
| Serial numbers | 11001, 11002, 11003, 11005, 11006, 11007, 11008, 11009, 11010, 11011, 11012, 11013, 11014, 11015, 11016, 11017, 11018, 11019, 11020, 11021, 11023, 11024, 11025, 11026, 11027 and 73 more |
| Model numbers | 31113.701, 31113.801 |
Product
The I-Cart is used to store, transport, and power video equipment used in medical procedures.
Reason for recall
The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke and black plastic material to leak from the cart chassis.
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-1240-2015. 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.