FDA Medical Device Recalls (openFDA)
LITTLE RAPIDS CORPORATION: EMS products from Graham Medical, SnugFit(R) Expandable Mattress Cover, Code 72930, UPC 1 07 47036 72930 3
- Recall number
- Z-0578-2018
- Recalling firm
- LITTLE RAPIDS CORPORATION
- Product
- EMS products from Graham Medical, SnugFit(R) Expandable Mattress Cover, Code 72930, UPC 1 07 47036 72930 3
- Status
- Terminated
- Initiated
- 2017-12-27
- Posted
- 2018-01-09
- Terminated
- 2018-07-30
- 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.
- Root cause
- Device Design
- Action
- The firm initiated their recall by email on 12/27/2017 to their direct consignees. The consignees were directed to report back with the number of products on hand for return and to notify their customers of the recall.
- Quantity
- 153 cases, 30 units in each case
- Distribution
- TX, CT, TN, MO, WI, FL, SD, MS, CA, MS
- Lot, serial or model codes
- Lot codes: 17871, 17971, 18071, and 18971
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KME
- Firm FEI
- 1000049086
- Firm city
- Green Bay
- Firm state
- WI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28