Public recall detail

Medline Convenience Kits Containing Cannula Components with Female Luer Lock Connectors

2026-10-01

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Health products Health product recall
Quick summary

Quick summary: Medline Convenience Kits Containing Cannula Components with Female Luer Lock Connectors. Reason: Health product recall. Category: Health products. Date: 2026-10-01.

Recommended action

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

Recall details

Quick summary: Medline Convenience Kits Containing Cannula Components with Female Luer Lock Connectors. Reason: Health product recall. Category: Health products. Date: 2026-10-01.

Official details

Affected product details

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

BrandMedline Industries, Lp
ProductMedline Convenience Kits Containing Cannula Components with Female Luer Lock Connectors
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82712

Affected products

ProductEM Pop Pack
Lot25JBB049
ModelDYNJ52921B
Serial number25JBB049
DescriptionEM Pop Pack
ProductPontage-LF
LotMore than 10 numbers, contact manufacturer.
ModelDYNJ58124D
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionPontage-LF
ProductPontage-LF
LotMore than 10 numbers, contact manufacturer.
ModelDYNJ58124B
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionPontage-LF
ProductPontage-LF
LotMore than 10 numbers, contact manufacturer.
ModelDYNJ58124C
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionPontage-LF

Issue

Specific item(s) and lot(s) of Medline Convenience Kits Containing Cannula Components with Female Luer Lock Connectors are being recalled. Medline has identified that the components do not conform to ISO 80369-7 dimensional requirements. The nonconforming dimensions may result in a loose, unstable, or detached Luer Lock connection and, in certain cases, may contribute to leaking or breaking during use, so customers will be directed to remove and destroy affected components.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesMedline Industries, Lp Three Lakes Drive, Northfield, Illinois, United States, 60093
Recall date2026-09-21
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82712
Background{}
CompaniesMedline Industries, Lp Three Lakes Drive, Northfield, Illinois, United States, 60093
AudiencesHealthcare
Source updated2026-10-01

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

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