Public recall detail

CTP - Tubing sets

2026-07-15

medium
Health products Health product recall
Quick summary

Quick summary: CTP - Tubing sets. Reason: Health product recall. Category: Health products. Date: 2026-07-15.

Recommended action

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

Recall details

Quick summary: CTP - Tubing sets. Reason: Health product recall. Category: Health products. Date: 2026-07-15.

Official details

Affected product details

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

BrandMaquet Cardiopulmonary Gmbh
ProductCTP - Tubing sets
IssueMedical devices - Sterility
Recall classType II
IdentificationRA-82328

Affected products

ProductCabaret 25 Kg
Lot3000419748
ModelBO-HQV 59206
Serial number3000419748
DescriptionCabaret 25 Kg
ProductPerfusion Pack
Lot3000407529
ModelBEQ-HQV 52700-1
Serial number3000407529
DescriptionPerfusion Pack
ProductPerfusion Pack
Lot3000415791
ModelBEQ-HQV 52700-1
Serial number3000415791
DescriptionPerfusion Pack
ProductPerfusion Pack
Lot3000460078
ModelBEQ-HQV 52700-1
Serial number3000460078
DescriptionPerfusion Pack
ProductPerfusion Pack
Lot3000491063
ModelBEQ-HQV 52700-1
Serial number3000491063
DescriptionPerfusion Pack
ProductPerfusion Pack
Lot3000468700
ModelBEQ-HQV 52700-1
Serial number3000468700
DescriptionPerfusion Pack
ProductPerfusion Pack
Lot3000460082
ModelBEQ-HQV 52700-1
Serial number3000460082
DescriptionPerfusion Pack
ProductPerfusion Pack
Lot3000407530
ModelBEQ-HQV 52700-1
Serial number3000407530
DescriptionPerfusion Pack
ProductPerfusion Pack
Lot3000491064
ModelBEQ-HQV 52700-1
Serial number3000491064
DescriptionPerfusion Pack
ProductHL Pack With HL 20
LotMore than 10 numbers, contact manufacturer.
ModelBEQ-HQV 46904
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionHL Pack With HL 20
ProductOHI Perfusion Pack
LotMore than 10 numbers, contact manufacturer.
ModelBO-HQV 55004
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionOHI Perfusion Pack

Issue

The manufacturer became aware of this issue due to six customer complaint reports. It was found that the sterile barrier was compromised, as the Tyvek lid was found opened prior to use. No harm to any person was reported. An internal investigation has confirmed that all affected products show a consistent similar defect pattern occurring at the same sealing area and were manufactured using the same tool. Therefore, this FSCA is limited to all sterile products within shelf-life manufactured using the same tool. Consignees will be asked to confirm receipt of the field action notification. Consignees will be asked to return all unused, affected sold product from consignee locations.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular Health products - Medical devices - General hospital and personal use
CompaniesMaquet Cardiopulmonary GmbhKehler Strasse 31, Rastatt, Germany, 76437
Recall date2026-06-29
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82328
Background{}
CompaniesMaquet Cardiopulmonary GmbhKehler Strasse 31, Rastatt, Germany, 76437
AudiencesHealthcare
Source updated2026-07-15

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

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