OFFICIAL-SOURCE RECALL · CANADA
pro+ Flat Deck Wide W/O X-Ray Recall: The UDI label for model p7924a13 incorrectly states
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- pro+ Flat Deck Wide W/O X-Ray
- Manufacturer
- See official notice
- Model number
- p7924a13
- Serial number / range
- number
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
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.
Hazard
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.
Official recall notice
pro+ Flat Deck Wide W/O X-Ray
Agency: Health Canada
Official publication date: August 27, 2026
Read the official CANADA_HEALTH recall notice →Scan products you own
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