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AUTOMATED MANIFOLD KIT (2015-12-22)
- Starting date:
- December 22, 2015
- Posting date:
- January 18, 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-56680
Affected Products
A. AUTOMATED MANIFOLD KIT
Reason
ACIST has received an increased frequency of field reports related to ingress of air into the manifold.
Affected products
A. AUTOMATED MANIFOLD KIT
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
14613
Companies
- Manufacturer
-
Acist Medical Systems Inc.
7905 FULLER ROAD
EDEN PRAIRIE
55344
UNITED STATES