Recall Z-3101-2017
Beckman Coulter Inc. · initiated June 20, 2017
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows for adaptation of the smear appearance and stain methodology according to user preferences. Blood smears produced by the Slidemaker portion of the DxH Slidemaker Stainer are moved to baskets for transfer to the Stainer portion by a robot arm. Microscopic examination of the stained blood smears can be used to help determine the hematologic status of a patient. A stained blood film: Allows for the differentiation of white blood cells, facilitates the characterization of red blood cells and platelets, and aids in the identification of blood components and cellular abnormalities.
Codes / lots: P/N A85371AA20; Catalog No. 775222
Reason for recall
The firm has identified that a fitting in some Slidemaker Stainer units may not completely seal after installation.
FDA-determined cause: Employee error
Action taken
Beckman Coulter sent an Urgent Medical Device Recall letter dated June 20, 2017. The notification advised consignees to immediately contact a Beckman Coulter representative if a leak is observed to schedule a service, to inspect reagent supply drawer for spills, and to follow best laboratory practices when using the device (including Personal Protective Equipment). Beckman Coulter indicates that the issue will be resolved with the replacement of the correct fitting on all impacted instruments. Labs were advised to notify all staff of the recall and to retain the notification. They were also instructed to forward the recall notice to all customers, if any product was further distributed, and to complete and return the Customer Response form within ten days of receiving the recall notification. Completed forms are to be sent back to the firm via email to Regulatory.Notifications@beckmancoulter.com. Regulatory Affairs Mail Code 31-B06. Questions can be directed to beckmancoulter.com or 800-526-7694. Consignees outside of the US are advised to contact their Beckman Coulter representative in the case that questions do arise.
Details
- Recall number
- Z-3101-2017
- Initiated
- June 20, 2017
- Terminated
- April 21, 2021
- Product code
- GKZ – Counter, Differential Cell
- Quantity
- 310 units
- Distribution
- Worldwide Distribution - USA (nationwide) Distribution to the states of : AL, AR, AZ, CA, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, NC, NJ, NV, NY, OH, OR, PA, RI, SC, TN, TX, VA, WA, and WV., and to the countries of : Australia, Brazil, Canada, Chile, China, Czech Republic, Denmark, France, Greece, Hong Kong, India, Israel, Italy, Japan, Morocco, Portugal, South Korea…
- Recalling firm
- Beckman Coulter Inc., Brea, CA