uTASWako DCP and uTASWako AFP-L3 (2018-07-27)
- Starting date:
- July 27, 2018
- Posting date:
- August 31, 2018
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-67640
Affected products
A. uTASWako DCP
B. uTASWako AFP-L3
Reason
Recall is due to incorrect information printed on labels and package inserts for the products.
Affected products
A. uTASWako DCP
Lot or serial number
contact manufacturer.
Model or catalog number
991-61401
995-60701
995-61301
999-61201
Companies
- Manufacturer
-
FUJIFILM Wako Pure Chemical Corporation
1-2 Doshomachi 3-Chome
Chuo-ku, Osaka
540-8605
JAPAN
B. uTASWako AFP-L3
Lot or serial number
contact manufacturer.
Model or catalog number
993-61101
997-60901
997-61001
997-61501
999-60601
Companies
- Manufacturer
-
FUJIFILM Wako Pure Chemical Corporation
1-2 Doshomachi 3-Chome
Chuo-ku, Osaka
540-8605
JAPAN