FDA Device recall Z-1552-2013
BC Hammock Mesh Sling (Medium), product number, 537005
- FDA Device
- Class II
- terminated
- Published 2013-06-26
On 2013-06-26 the FDA classified a Class II recall of BC Hammock Mesh Sling (Medium), product number, 537005 by Prism Medical Services Usa, citing the product does not meet the firm's size standards, the product was produced in the incorrect size.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1552-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-23 |
| Published | 2013-06-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Prism Medical Services Usa |
| Distribution | US |
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.
Reason
The product does not meet the firm's size standards, the product was produced in the incorrect size.
Identifiers
| code_info | Lot: PHM000444, PHM000445, PHM000446, PHM000447, PHM000634, PHM000635, PHM000636, PHM000637, PHM000294 and PHM000638. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1552-2013%22
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