This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
Trellis 6 & Trellis 8 Peripheral Infusion System (2015-03-18)
- Starting date:
- March 18, 2015
- Posting date:
- April 29, 2015
- 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-53121
Recalled products
- Trellis 6 & Trellis 8 Peripheral Infusion System
Reason
Covidien is issuing a voluntary recall of all Trellis 6 and Trellis 8 peripheral infusion systems due to potential for a sterility breach of the outer packaging or pouch material. A breach of the outer pouch may compromise the outside surface sterility of the inner pouch and does not directly affect the sterility of the device components within the inner pouch.
Affected products
A. Trellis 6 & Trellis 8 Peripheral Infusion System
Lot or serial number
All lots.
Model or catalog number
- BVT608010
- BVT608030
- BVT612010
- BVT612030
- BVT808015
- BVT808030
- BVT812015
- BVT812030
Companies
- Manufacturer
-
Covidien LLC
15 Hampshire Street
Mansfield
Massachusetts
UNITED STATES