Beckman Coulter Inc Power Processor Aliquot Tube Labels Part 800255 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Power Processor Aliquot Tube Labels Part 800255
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
Lots 21045673, 2105246, 21361906.
Products Sold
Lots 21045673; 2105246; 21361906.
Beckman Coulter Inc is recalling Power Processor Aliquot Tube Labels Part 800255 due to Labels are missing an expiration date and storage instructions, increasing the likelihood that they will not be used by the expiration date or may be . Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: distribution information, corrective action details.
Reason for Recall
As stated by FDA
Labels are missing an expiration date and storage instructions, increasing the likelihood that they will not be used by the expiration date or may be stored under conditions that would cause adhesive failure and loss of identity of sample or aliquot during testing.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026