DxM 1040 MicroScan WalkAway Instrument REF B1018-440
Reported: May 25, 2022 Initiated: October 21, 2019 #Z-1085-2022
Product Description
DxM 1040 MicroScan WalkAway Instrument REF B1018-440
Reason for Recall
WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10 ampere
Details
- Recalling Firm
- Beckman Coulter Inc.
- Units Affected
- 40 systems
- Distribution
- Worldwide distribution - U.S. Nationwide distribution in the states of Alaska, Arkansas, California, Colorado, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maine, Maryland, Michigan, Minnesota, Missouri, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Pennsylvania, Tennessee, Texas, Utah, Vermont, Virginia, and Washington. The countries of Belgium, Brazil, Colombia, Germany, Hong Kong, Indonesia, Italy, Japan, Paraguay, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Spain, Switzerland, Taiwan, United Arab Emirates, Vietnam and Yemen.
- Location
- Brea, CA
Frequently Asked Questions
What product was recalled? ▼
DxM 1040 MicroScan WalkAway Instrument REF B1018-440. Recalled by Beckman Coulter Inc.. Units affected: 40 systems.
Why was this product recalled? ▼
WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10 ampere
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 25, 2022. Severity: Moderate. Recall number: Z-1085-2022.
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