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Medscape Medical News 2007. © 2007 Medscape
September 11, 2007 — A global alert has been issued by Abbott to warn
users that certain diabetic blood glucose meters may not function
properly if dropped on a hard surface, the US Food and Drug
Administration told healthcare professionals today.
The notification applies to Precision Xtra, Optium, ReliOn Ultima, Rite
Aid, and Kroger brand meters manufactured after January 31, 2007,
according to an alert from MedWatch, the FDA's safety information and
adverse event reporting program.
Dropping these recently produced units may cause part of the display to
be jarred or disconnected, rendering the screen partially or totally
blank. Users unable to view their test results may be at risk for hypo-
or hyperglycemia, the company said.
Patients should be advised to keep their glucose meters in the wallet
provided to offer additional protection. If the unit is dropped, its
display must be checked immediately according to instructions in the
users guide; malfunctioning units must not be used.
Additional information and free replacement meters may be obtained by
contacting the company at 1-877-844-4404.
Healthcare professionals are encouraged to report ceftriaxone-related
adverse events to the FDA's MedWatch reporting program by phone at
1-800-FDA-1088, by fax at 1-800-FDA-0178, online at
http://www.fda.gov/medwatch, or by mail to 5600 Fishers Lane, Rockville,
MD 20852-9787.
Susan