FDA recall record

Estill Medical Technologies Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra recall — FDA Z-0101-2015

Estill has discovered that a fully discharged Ultra Battery 1 (TA-UB1) will reach 96.9% of its capacity during a 60 minute charging period. If you have a…

Class IIclassification
Z-0101-2015official record ID
Oct 29, 2014report date

Recall record at a glance

Official recordZ-0101-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEstill Medical Technologies, Inc.
Report dateOct 29, 2014
Recall initiation dateJul 25, 2014
Quantity6,886
LocationDallas, TX, United States

Official product description

Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery 1 (TA-UB1) is a rechargeable power source for the Thermal Angel Blood and IV Fluid Infusion Warmer. The TA-UB1 battery was designed to provide sufficient power for the Thermal Angel to warm and deliver one liter of blood or IV fluid infusion to a trauma patient.

Why the product was recalled

Estill has discovered that a fully discharged Ultra Battery 1 (TA-UB1) will reach 96.9% of its capacity during a 60 minute charging period. If you have a fully discharged Ultra Battery 1 (TA-UB1), in order to achieve a 100% of charge capacity you should charge it for a period of 90 minutes. In addition, the charging voltage range of 10-36V specified on the Ultra Battery 1 (TA-UB1) label and in t

Distribution information

Worldwide Distribution - USA (nationwide) and Internationally to Serbia.

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

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