Public recall detail

Transfer Set (Minicap Extended Life Pd Transfer Set With Twist Clamps)

2024-10-31

medium
Recall Safety notice
Quick summary

Quick summary: Transfer Set (Minicap Extended Life Pd Transfer Set With Twist Clamps). Date: 2024-10-31.

Recommended action

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

Recall details

Quick summary: Transfer Set (Minicap Extended Life Pd Transfer Set With Twist Clamps). Date: 2024-10-31.

Official details

Affected product details

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

BrandBaxter Healthcare Corporation
ProductTransfer Set (Minicap Extended Life Pd Transfer Set With Twist Clamps)
IssueMedical devices - Performance
Recall classType II
IdentificationRA-76420

Affected products

ProductTransfer Set (Minicap Extended Life Pd Transfer Set With Twist Clamp – Extra Short)
LotLot H23J10051 and higher
Model5C4483
Serial numberLot H23J10051 and higher
DescriptionTransfer Set (Minicap Extended Life Pd Transfer Set With Twist Clamp – Extra Short)
ProductTransfer Set (Minicap Extended Life Pd Transfer Set With Twist Clamp)
LotLot H24G31023 and higher Lot H23J16074 and higher
Model5C4482 5C4482A
Serial numberLot H24G31023 and higher Lot H23J16074 and higher
DescriptionTransfer Set (Minicap Extended Life Pd Transfer Set With Twist Clamp)

Issue

Baxter Healthcare Corporation is issuing a safety alert for the Minicap Extended Life Pd Transfer Sets listed due to an increase in complaints related to separation of the connector or spike from the main body of the transfer set. These separations may occur while connecting or disconnecting from the patient line, however as the tubing remains connected to the connector or spike during a separation, the sterile fluid path is maintained and there is no risk of microbial contamination that will result from the separation itself. Recall Start Date: October 21, 2024

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Healthcare
CategoryHealth products - Medical devices - Gastroenterology and urology
CompaniesBaxter Healthcare Corporation 1 Baxter Parkway, Deerfield, Illinois, United States, 60015
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-76420
Background{}
CompaniesBaxter Healthcare Corporation 1 Baxter Parkway, Deerfield, Illinois, United States, 60015
AudiencesGeneral public Healthcare
Source updated2024-10-31

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

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