Public recall detail

VIRTUTRAX KIT

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Recall Safety notice
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Quick summary: VIRTUTRAX KIT.

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Recall details

Quick summary: VIRTUTRAX KIT.

Official details

Affected product details

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

BrandCIVCO MEDICAL INSTRUMENTS CO., INC
ProductVIRTUTRAX KIT
IssueMedical devices - Mechanical defect
Recall classType II
IdentificationRA-63533

Affected products

ProductVIRTUTRAX KIT
LotA120641, SN#5HB20Z2010 A132258, SN#5HB20Z2020 A132258, SN#5HB2122028 A132258, SN#5HB2122034 A132471, SN#5HB2172070
Model610-1059
Serial numberA120641, SN#5HB20Z2010 A132258, SN#5HB20Z2020 A132258, SN#5HB2122028 A132258, SN#5HB2122034 A132471, SN#5HB2172070
DescriptionVIRTUTRAX KIT

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Health professionals Hospitals
CategoryHealth products - Medical devices - General and plastic surgery
CompaniesCIVCO MEDICAL INSTRUMENTS CO., INC. DBA CIVCO, 102 FIRST STREET SOUTH, KALONA IOWA, UNITED STATES 52247
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-63533
Background{}
CompaniesCIVCO MEDICAL INSTRUMENTS CO., INC. DBA CIVCO, 102 FIRST STREET SOUTH, KALONA IOWA, UNITED STATES 52247
AudiencesGeneral public Health professionals Hospitals
Source updated2021-10-29

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

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