FDA recall record

Draeger Medical PS500 of an IACS Workstation Critical Care (Evita Infinity V500) recall — FDA Z-2343-2015

The battery capacity of the optional PS500 of an IACS Workstation Critical Care (Evita Infinity V500) did not last as long as expected.

Class Iclassification
Z-2343-2015official record ID
Aug 26, 2015report date

Recall record at a glance

Official recordZ-2343-2015
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmDraeger Medical, Inc.
Report dateAug 26, 2015
Recall initiation dateJul 13, 2015
Quantity2081
LocationTelford, PA, United States

Official product description

PS500 of an IACS Workstation Critical Care (Evita Infinity V500); intended for the ventilation of adult, pediatric and neonatal patients.

Why the product was recalled

The battery capacity of the optional PS500 of an IACS Workstation Critical Care (Evita Infinity V500) did not last as long as expected.

Distribution information

Nationwide Distribution.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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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