Health product recall

Teleflex Disposable Aortic Punch (2020-01-14)

Starting date:
January 14, 2020
Posting date:
January 31, 2020
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-72223

Last updated: 2020-01-31

Affected Products

Teleflex Disposable Aortic Punch

Reason

Teleflex is recalling the above product as there is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.

Affected products

Teleflex Disposable Aortic Punch

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number
  • DP-28K
  • DP-36K
  • DP-40K
  • DP-44K
  • DP-48K
  • DP-52K
  • DP-56K
  • DP-60K
  • MDP-28K
  • MDP-36K
  • MDP-40K
  • MDP-44K
  • MDP-48K
  • MDP-52K
  • MDP-56K
  • MDP-60K
Companies
Manufacturer

Teleflex Medical

3015 Carrington Mill BLVD

Morrisville

27560

North Carolina

UNITED STATES