Public recall detail

SEMA 3

2026-07-16

medium
Health products Health product recall
Quick summary

Quick summary: SEMA 3. Reason: Health product recall. Category: Health products. Date: 2026-07-16.

Recommended action

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

Recall details

Quick summary: SEMA 3. Reason: Health product recall. Category: Health products. Date: 2026-07-16.

Official details

Affected product details

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

BrandSchiller AG
ProductSEMA 3
IssueMedical devices - Device compatibility
Recall classType II
IdentificationRA-82336

Affected products

ProductSEMA 3
LotNot applicable.
Model6020.009411
Serial numberNot applicable.
DescriptionSEMA 3
ProductSEMA 3
LotNot applicable.
Model6020.012099
Serial numberNot applicable.
DescriptionSEMA 3
ProductSEMA 3
LotNot applicable.
Model6020.009412
Serial numberNot applicable.
DescriptionSEMA 3

Issue

When an ECG is aquired with DEFIGARD Touch 7 or ARGUS PRO LifeCare 3 with the newest software, there might be a discrepancy between the aquiring device and SEMA. This results from inadequate processing by SEMA to an already filtered signal. SEMA should be updated to version 25.10.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceIndustry
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesSchiller AgAltgasse 68, Baar, Zug, Switzerland, 6341
Recall date2026-07-08
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82336
Background{}
CompaniesSchiller AgAltgasse 68, Baar, Zug, Switzerland, 6341
AudiencesIndustry
Source updated2026-07-16

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

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