ABL800 FLEX model number 393-800 and 393-801, UDI:(01)05700693938004
FDA Recall Z-1836-2020 · Posted None
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Recalling FirmRadiometer Medical ApS
Recall StatusOpen, Classified
Product CodeCHL
Date Initiated2020-03-06
Product Quantity2 units
Reason for Recall
Through internal investigation is has been determined that an incorrect component was used within the power supply. The incorrect component may cause a short circuit within the power supply resulting in a delay in treatment. The delay could result in a range of risk from cyanosis and low blood pressure to cardiac arrhythmias and severe impairment of cardiac function.
Firm Action
On 3/5/2020 a "Urgent: Medical device Recall" letter was hand delivered to effective consignees. In addition to providing information on the recall products, the customer notification as consignees to take the following actions:
Solution provided by Radiometer:
1. Your Radiometer representative will exchange the power supply of your ABL800 analyzer at the earliest convenience.
Your Actions:
1. Cease using the affected ABL800 analyzer and put it on quarantine.
2. Shut down the affected ABL800 analyzer and disconnect the power cord.
3. Complete the Recall Response Form (last page of this letter) and submit to your Radiometer representative
4. If you have any questions, please contact us at 1-800-736-0600 option 1, Monday Friday 9am EST to 7pm EST.
Root Cause
Component design/selection
Distribution Pattern
US: in the state of California
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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