FDA recall record

CareFusion 303 Alaris PC units, Model No. 8015 recall — FDA Z-1311-2015

CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a…

Class IIclassification
Z-1311-2015official record ID
Apr 1, 2015report date

Recall record at a glance

Official recordZ-1311-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCareFusion 303, Inc.
Report dateApr 1, 2015
Recall initiation dateMar 12, 2015
Quantity56,015 units
LocationSan Diego, CA, United States

Official product description

Alaris PC units, Model No. 8015. Infusion pump.

Why the product was recalled

CareFusion is recalling the Alaris PC unit because of an error code. The error code may occur upon power on during the "Power-On Self Test" due to a keypad issue.

Distribution information

Worldwide Distribution - USA (nationwide), Canada, European Union, Singapore and Australia.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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