Class II — LITTLE RAPIDS CORPORATION
| Recalling firm | LITTLE RAPIDS CORP. |
|---|---|
| Registered facility | Little Rapids Corporation (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The secondary supplier provided material was within specification but did not meet our design needs compared to the primary manufacturer. The product is designed for patient transfer, not lifting. However, we recognize that the product may be utilized outside of its intended design scope, and lifting may occur. Lifting could lead tearing of the equipment cover and the potential for patient falling through. |
| Product | EMS products from Graham Medical, SnugFit(R) Expandable Mattress Cover, Code 72930, UPC 1 07 47036 72930 3 |
| Quantity | 153 cases, 30 units in each case |
| Distribution | TX, CT, TN, MO, WI, FL, SD, MS, CA, MS |
| Initiated | 2017-12-27 |
| Classified | 2018-02-09 |
| Terminated | 2018-07-30 |
| Recall number | Z-0578-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — LITTLE RAPIDS CORPORATION (Z-0578-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/78899/
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