Health product recall

Captus 3000 and 700 (2018-11-04)

Starting date:
November 4, 2018
Posting date:
November 28, 2018
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-68432

Affected products

  1. Captus 3000
  2. Captus 700

Reason

Capintec received reports of arm failures on Captus 3000 systems shipped in 2011-2012. This malfunction will cause the arm and collimator assembly (45 pounds) to fall to its lowest position, which has the potential for injury if the collimator comes in contact with operator or patient.

Affected products

A. Captus 3000

Lot or serial number
  • 901086
  • 901192
  • 901308
  • 901309
Model or catalog number
  • 5430-0076
Companies
Manufacturer

Capintec Inc.

7 Vreeland Rd

Florham Park

07932

New Jersey

UNITED STATES


B. Captus 700

Lot or serial number
  • 700018
Model or catalog number
  • 5430-3137
Companies
Manufacturer

Capintec Inc.

7 Vreeland Rd

Florham Park

07932

New Jersey

UNITED STATES