Public recall detail

Stryker ProCuity Beds

2024-05-08

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Recall Safety notice
Quick summary

Quick summary: Stryker ProCuity Beds. Date: 2024-05-08.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Stryker ProCuity Beds. Date: 2024-05-08.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandStryker Medical
ProductStryker ProCuity Beds
IssueMedical devices - Performance
Recall classType II
IdentificationRA-75497

Affected products

ProductStryker ProCuity Beds
LotMore than 10 numbers, contact manufacturer.
Model3009PX-LE-400 300900000000 3009QC-P1 3009PX-LEX-400
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionStryker ProCuity Beds

Issue

Stryker has identified that the manufacturing records for certain ProCuity beds are missing test values for electrical safety tests as required by IEC 62353:2014. As a result of the missing test data, the impacted units are not compliant to the above standard. Therefore, Stryker is initiating this voluntary recall to perform the necessary testing and documentation in the field. Recall start date : April 29, 2024

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesStryker Medical 3800 E Centre Avenue, Portage, Michigan, United States, 49002
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-75497
Background{}
CompaniesStryker Medical 3800 E Centre Avenue, Portage, Michigan, United States, 49002
AudiencesHealthcare
Source updated2024-05-08

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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