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Bioplant (2015-11-05)
- Starting date:
- November 5, 2015
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-55984
Affected Products
Bioplant
Reason
2015/11/03: During an audit, the company discovered that a CE mark and notified body number were present in some of the Bioplant labelling materials. There is no safety risk to health.
Affected products
Bioplant
Lot or serial number
- 216112 - 2685295 (18 syringes)
- 216112 - 2720970 (6 syringes)
- 216112 - 2763763 (6 syringes)
- 216112 - 2763764 (18 syringes)
- 216132 - 2649171 (4 syringes)
- 216132 - 2685297 (4 syringes)
- 216132 - 2720971 (4 syringes)
- 216132 - 2746762 (4 syringes)
- 216132 - H005876 (12 syringes)
Model or catalog number
- 216112
- 216132
Companies
- Manufacturer
-
Kerr Corporation
1717 West Collins Ave.
Orange
92867
California
UNITED STATES