Class 4 caution in use-Freeflex/Steriflex No. 11 Hartmann's solution

Fresenius Kabi Limited has informed the MHRA of a labelling error on the packaging of Hartmann’s solution for Injection BP as Steriflex No.11 or freeflex.

MHRA Drug alert date: 24th July 2024

MHRA drug alert link https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-fresenius-kabi-limited-hartmanns-solution-for-injection-bp-as-steriflex-no-11-or-freeflex-el-24-a-slash-31?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=266c16df-6328-44c8-bc25-a79181e2bf0f&utm_content=immediately

This is a caution in use only we are not accepting stock returns

Further Information

For more information or medical information queries please email
Medical.Information-UK@fresenius-kabi.com or telephone +44 (0) 1928533575.

For stock control enquiries please contact FK.complaints-uk@fresenius-kabi.com or telephone +44 (0) 1928 533758.