Public recall detail

Modular Cathcart Fracture Head

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Recall Safety notice
Quick summary

Quick summary: Modular Cathcart Fracture Head.

Recommended action

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

Recall details

Quick summary: Modular Cathcart Fracture Head.

Official details

Affected product details

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

BrandDepuy Orthopaedics, Inc.
ProductModular Cathcart Fracture Head
IssueMedical devices - Labelling and packaging
Recall classType II
IdentificationRA-64293

Affected products

ProductModular Cathcart Fracture Head Hip Ball (Endoprosthesis)
LotAll lots.
Model1363-43-000 1363-46-000 1363-50-000 1363-53-000 1363-44-000 1363-51-000 1363-48-000 1363-49-000 1363-42-000 1363-45-000 1363-47-000 1363-60-000 1363-58-000 1363-54-000 1363-41-000 1363-52-000 1363-56-000
Serial numberAll lots.
DescriptionModular Cathcart Fracture Head Hip Ball (Endoprosthesis)
ProductModular Cathcart Fracture Head Tapered Spacer Articul-Eze Taper (Endopros.)
LotAll lots.
Model1363-14-000
Serial numberAll lots.
DescriptionModular Cathcart Fracture Head Tapered Spacer Articul-Eze Taper (Endopros.)

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Orthopaedics
CompaniesDepuy Orthopaedics, Inc. 700 Orthopaedic Drive, Warsaw, Indiana, United States, 46582
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-64293
Background{}
CompaniesDepuy Orthopaedics, Inc. 700 Orthopaedic Drive, Warsaw, Indiana, United States, 46582
AudiencesHealthcare
Source updated2022-06-20

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

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