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Health product recall

Penadapt (2014-03-20)

Starting date:
March 20, 2014
Posting date:
April 14, 2014
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Disease
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-39021

Recalled Products

Penadapt

Reason

Manufacturer has become aware of a potential sterility breach and the presence of foreign particulates/metal shavings in the packaging.

Affected products

Penadapt 

Lot or serial number

More than 10 numbers, contact manufacturer 

Model or catalog number

0702-045-027

Companies
Manufacturer
Stryker Instruments
4100 East Milham Ave.
Kalamazoo
49001
Michigan
UNITED STATES