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Health product recall

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Starting date:
October 4, 2016
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-60680

Affected Products

Reason

This voluntary recall is being conducted due to the potential for compromise of the package resulting in a breach of the sterile barrier. The use of products with this packaging defect may increase risk of infection.

Affected products

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Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

21-345

Companies
Manufacturer
Covidien LLC
15 Hampshire Street
Mansfield
02048
Massachusetts
UNITED STATES