Quick summary
Quick summary: Hank Cervical Dilator. Date: 2024-12-05.
Public recall detail
Hank Cervical Dilator
2024-12-05
Recall
Safety notice
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Hank Cervical Dilator. Date: 2024-12-05.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandCoopersurgical Inc.
ProductHank Cervical Dilator
IssueMedical devices - Labelling and packaging
Recall classType II
IdentificationRA-76644
Affected products
ProductHank Cervical Dilator
Lot00888937017083 00888937017106 00888937017113 00888937017090
Model61201 61204 61202 61203
Serial number00888937017083 00888937017106 00888937017113 00888937017090
DescriptionHank Cervical Dilator
Issue
The size indicated on the box labels did not match the expected size of the part number. Recall start date: November 19, 2024
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Healthcare Industry
CategoryHealth products - Medical devices - Obstetrics and gynaecology
CompaniesCoopersurgical Inc. 95 Corporate Drive, Trumbull, Connecticut, United States, 06611
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-76644
Background{}
CompaniesCoopersurgical Inc. 95 Corporate Drive, Trumbull, Connecticut, United States, 06611
AudiencesGeneral public Healthcare Industry
Source updated2024-12-05
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
FAQ
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Product images
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