BfArM - Federal Institute for Drugs and Medical Devices

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Product group Injections / Infusions / Transfusions / Dialysis
Reference 01133/05

The company Baxter Deutschland GmbH notified users of a recall of the 6060 Pumps due to a possible incorrect calibration procedure for the 'air in line' alarm. Responsables are requested either not to use the devices or to apply an infusion set with 1,2μ filter. According to Baxter only users in Germany and France are concerned.

Advisory Notice is only available in German language.

Baxter recalls the 6060 Pumps , Download_VeroeffentlichtAm_EN PDF, 115KB,

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