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Various Covidien Sterile Dressings (2017-03-03)
- Starting date:
- March 3, 2017
- Posting date:
- April 13, 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-62956
Affected Products
- Kerlix Super Sponge Saline Dressing
- Curity Sodium Chloride Dressing
- Curity Wet Dressing
- Curity Saline Dressing
- Covidien Curity Eye Pad
- Manufacturer
-
Covidien LLC
15 Hampshire Street
Mansfield
02048
Massachusetts
UNITED STATES
- Manufacturer
-
Covidien LLC
15 Hampshire Street
Mansfield
02048
Massachusetts
UNITED STATES
- Manufacturer
-
Covidien LLC
15 Hampshire Street
Mansfield
02048
Massachusetts
UNITED STATES
- Manufacturer
-
Covidien LLC
15 Hampshire Street
Mansfield
02048
Massachusetts
UNITED STATES
- Manufacturer
-
Covidien LLC
15 Hampshire Street
Mansfield
02048
Massachusetts
UNITED STATES
Reason
This voluntary recall is being conducted due to the potential for the sterile packaging to be compromised. The use of products with this condition may result in a potentially increased risk for infection. There have been no reports of infection associated with this issue.
Affected products
A. Kerlix Super Sponge Saline Dressing
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
3338
Companies
B. Curity Sodium Chloride Dressing
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
3339
Companies
C. Curity Wet Dressing
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
3337
Companies
D. Curity Saline Dressing
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
3606
Companies
E. Covidien Curity Eye Pad
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
91650
Companies