Beckman Coulter Inc. 2022-05-25 Health serious FDA
Health · FDA · Recall #FDA-Z-1086-2022
DxM 1096 MicroScan WalkAway Instrument REF B1018-496 Recall
Issued May 25, 2022 · Beckman Coulter Inc.
In May 2022, Beckman Coulter Inc. recalled the DxM 1096 MicroScan WalkAway Instrument REF B1018-496, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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
What you should do
- 1 Stop using DxM 1096 MicroScan WalkAway Instrument REF B1018-496 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Beckman Coulter Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Beckman Coulter Inc.
- Category
- Health
- Recall date
- May 25, 2022
- Units affected
- Not reported
- Sold at
- Worldwide distribution - U.S. Nationwide distribution in the states of Alaska, Arkansas, California, Colorado, District of Columbia, Florida
- Recall number
- FDA-Z-1086-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Beckman Coulter Inc. has 4 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.