Skip to the content

FDA Medical Device Recalls (openFDA)

Prism Medical Services USA: BC Hammock Mesh Sling (Junior), product number, 537005. Product Usage: The fabric sling is used for the transfer of a patient, for example from a bed to a wheelchair.

Recall number
Z-1555-2013
Recalling firm
Prism Medical Services USA
Product
BC Hammock Mesh Sling (Junior), product number, 537005. Product 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
1 sling
Distribution
Worldwide distribution: USA (nationwide) including states of: CA, IL, OH, and TX. and country of: Canada.
Lot, serial or model codes
Lot: PHM000524.
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

Search this register