FDA Medical Device Recalls (openFDA)
Prism Medical Services USA: BC Hammock Mesh Sling (Medium), product number, 537005. Product Usage: Usage: The fabric sling is used for the transfer of a patient, for example from a bed to a wheelchair.
- Recall number
- Z-1552-2013
- Recalling firm
- Prism Medical Services USA
- Product
- BC Hammock Mesh Sling (Medium), product number, 537005. Product Usage: Usage: The fabric sling is used for the transfer of a patient, for example from a bed to a wheelchair.
- Status
- Terminated
- Initiated
- 2013-05-23
- Posted
- 2013-06-19
- Terminated
- 2013-11-25
- Reason
- The product does not meet the firm's size standards, the product was produced in the incorrect size.
- Root cause
- Employee error
- Action
- Prism Medical contacted their US consignees on May 28, 2013 with an e-mail notification of the recall. The notification explained the Field Safety Notice Letter dated May 22, 2013. The notice identified the affected product, problem and actions to be taken. Customers were instructed to contact Customer Service at Prism Medical to receive a return goods authorization to replace the affected product at no charge. For questions call 905-850-9003 Ext. 249.
- Quantity
- 10 slings
- Distribution
- Worldwide distribution: USA (nationwide) including states of: CA, IL, OH, and TX. and country of: Canada.
- Lot, serial or model codes
- Lot: PHM000444, PHM000445, PHM000446, PHM000447, PHM000634, PHM000635, PHM000636, PHM000637, PHM000294 and PHM000638.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FSA
- Firm FEI
- 3007802293
- Firm city
- Maryland Heights
- Firm state
- MO
- 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