Recall MonitorHealth Products
pro+ Flat Deck Wide W/O X-Ray
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - General hospital and personal use
Product: pro+ Flat Deck Wide W/O X-Ray
Issue: Medical devices - Device compatibility
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
Products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| pro+ Flat Deck Wide W/O X-Ray | SN A325BP9877 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A325BP9879 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A212BP5484 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A212BP5483 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A325BP9878 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A325BP9859 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A212BP5457 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A212BP5474 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A268BP7555 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A315BP9277 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A212BP5459 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A212BP5475 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A212BP5473 | P7924A13 |
| pro+ Flat Deck Wide W/O X-Ray | SN A325BP9858 | P7924A13 |
Issue
The UDI label for model p7924a13 incorrectly states the product description as "Pro+ 40 MRS surface with x-ray" instead of the actual configuration, which is "Pro+ 36 MRS surface." Model p7924a13 should be used with 36" width bed frames and not 40" width bed frames. These discrepancies in labeling do not align with the approved product or product specifications and may lead to incorrect product identification or selection, potentially resulting in use with an incompatible bed frame.