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Weck Vista Products (2014-03-24)
- Starting date:
- March 24, 2014
- Posting date:
- June 5, 2014
- 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-39877
Recalled Products
a) Weck Vista Products
b) Weck Vista Products
c) Weck Vista Products
d) Weck Vista products
e) Weck Vista product
Affected products
a) Weck Vista Products
Lot or serial number
01L1200353
Model or catalog number
405933
410944
Companies
- Manufacturer
-
Teleflex Medical
2917 Wreck Drive,
Research Triangle Park
27709
North Carolina
UNITED STATES
b) Weck Vista Products
Lot or serial number
01J1200461
01J1200462
01K1200266
01K1200611
Model or catalog number
405910
405912
Companies
- Manufacturer
-
Teleflex Medical
2917 Wreck Drive,
Research Triangle Park
27709
North Carolina
UNITED STATES
c) Weck Vista Products
Lot or serial number
01A1300178 01K1200728
01K1200600 01K1200066
01L1200355 01A1300202
Model or catalog number
410944
410944L
412944
412944L
Companies
- Manufacturer
-
Teleflex Medical
2917 Wreck Drive,
Research Triangle Park
27709
North Carolina
UNITED STATES
d) Weck Vista products
Lot or serial number
01A1300170
01J1200009 01J1200234
01K1200378 01K1200621
01M1200251 01A1300201
Model or catalog number
405910R
405912R
Companies
- Manufacturer
-
Teleflex Medical
2917 Wreck Drive,
Research Triangle Park
27709
North Carolina
UNITED STATES
e) Weck Vista product
Lot or serial number
01A1300559
Model or catalog number
405912RC
Companies
- Manufacturer
-
Teleflex Medical
2917 Wreck Drive,
Research Triangle Park
27709
North Carolina
UNITED STATES