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Health product recall

EDS Light Suspension, Central Axis For Visum Led Surgical Light

Starting date:
March 7, 2017
Posting date:
March 24, 2017
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-62792

Reason

Stryker has become aware that there is a remote likelihood that the EDS Light Suspension, Central Axis may have an insufficiently assembled joint in the suspension. The EDS Systems have redundant connections throughout the suspensions. If the EDS Light Suspension, Central Axis falls, it could potentially cause serious injuries to healthcare providers and/or patients. To date, there have been no adverse events reported for this issue.

Affected products

EDS Light Suspension, Central Axis For Visum Led Surgical Light

Lot or serial number

0682-001-229

0682-001-286

0682-001-298

0682-001-300

0682-001-432

0682-001-433

0682-001-434

0682-001-435

Model or catalog number

0682-001-229

0682-001-286

0682-001-298

0682-001-300

0682-001-432

0682-001-433

0682-001-434

0682-001-435

Companies

Manufacturer

Stryker Communications

1410 Lakeside Pkwy #100

Flower Mound

75028

Texas

UNITED STATES