Health product recall

pro+ Flat Deck Wide W/O X-Ray

Brand(s)
Last updated

Summary

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

Affected 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.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Hill-Rom, Inc.

1069 State Route 46 East, Batesville, Indiana, United States, 47006-9167

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82532

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