Public recall detail

1788 4K Camera

2026-08-05

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Health products Health product recall
Quick summary

Quick summary: 1788 4K Camera. Reason: Health product recall. Category: Health products. Date: 2026-08-05.

Recommended action

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

Recall details

Quick summary: 1788 4K Camera. Reason: Health product recall. Category: Health products. Date: 2026-08-05.

Official details

Affected product details

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

BrandSTRYKER ENDOSCOPY, A DIV. OF STRYKER CORP. DBA STRYKER ENDOSCOPY
Product1788 4K Camera
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82442

Affected products

Product1788 4K Camera Head, C-Mount With Advanced Imaging Modality
Lot23H519774
Model1788210105
Serial number23H519774
Description1788 4K Camera Head, C-Mount With Advanced Imaging Modality
Product1788 4K Camera Control Unit With Advanced Imaging Modality
LotNot applicable
Model1788010000
Serial numberNot applicable
Description1788 4K Camera Control Unit With Advanced Imaging Modality
Product1788 4K Camera Head With Integrated Coupler With Advanced Imaging Modality
LotMore than 10 numbers, contact manufacturer.
Model1788610122
Serial numberMore than 10 numbers, contact manufacturer.
Description1788 4K Camera Head With Integrated Coupler With Advanced Imaging Modality

Issue

Stryker Endoscopy has received an increase in complaints for 1788 out of box failures due to bent connection pins. The bent pin may also damage the mating connector in the CCU. Stryker has investigated and identified a service repair issue which contributed to the bent pins noted with these devices.

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 Health products - Medical devices - Gastroenterology and urology
CompaniesStryker Endoscopy, A Div. Of Stryker Corp. Dba Stryker Endoscopy5900 Optical Court, San Jose, California, United States, 95138
Recall date2026-07-27
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82442
Background{}
CompaniesStryker Endoscopy, A Div. Of Stryker Corp. Dba Stryker Endoscopy5900 Optical Court, San Jose, California, United States, 95138
AudiencesHealthcare
Source updated2026-08-05

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

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