Abbott Alcyon 300 Analyzer 535 units Class II

1/13/00 Class II

PRODUCT

Alycon Analyzers, automated chemistry analyzers for in-vitro diagnostic
use: a) Alycon Analyzer 300; b) Alycon Analyzer 300i. Recall #Z-
462/463-0.

REASON

Software program errors cause incorrect association between patient and
the patient results.

CODE

All codes.
MANUFACTURER

Abbott Laboratories, Inc., Irving, Texas.

RECALLED BY

Manufacturer, by letter dated January 13, 2000. Firm-initiated recall
ongoing.

DISTRIBUTION

Nationwide and Puerto Rico.

QUANTITY

535 analyzers distributed in the United States from 5/1/98 to 12/1/99.

About the author

Amy enjoys researching and writing about developments in medical technology and how that intersects with US law. She received her J.D. from the University of Florida Levin College of Law in 2020 and now works as a Regulatory Associate for SoftwareCPR®, a general-purpose regulatory consulting firm that is recognized globally for their expertise with standards and national regulations pertaining to medical device, mobile medical app, and HealthIT software.

What’s New

FDA:  Exemptions, Variances, and Alternate Forms of Adverse Event Reporting for Medical Devices

Manufacturers, importers, and user facilities can request an exemption or variance from any or all of the medical device reporting requirements in 21 CFR Part 803.  Read more:  https://www.fda.gov/medical-devices/medical-device-reporting-mdr-how-report-medical-device-problems/exemptions-variances-and-alternate-forms-adverse-event-reporting-medical-devices

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