Class 4 medicine recall 25 January 2022

Class 4 Medicines Defect Information: Fresenius Kabi Limited, Kabiven Emulsion for Infusion

Yes – this has been recalled
The problem
Fresenius Kabi Limited have identified an error on the infusion bag packaged in certain batches.
What to do
Check the batch number on your pack against the list below. Do not stop taking a prescribed medicine without talking to your pharmacist, GP or prescriber first – they can check your supply and swap it if needed.
Source: Medicines and Healthcare products Regulatory Agency (MHRA) Official notice ↗

MDR Number

MDR 117-01/22

Company name

Fresenius Kabi Limited

Product description

Kabiven Emulsion for Infusion PL 08828/0131

Batch Number Expiry Date Pack Size First Distributed
10PC9374 28 Feb 2022 4 x 2053 ml 3-chamber infusion bag 05 May 2020
10PE3357 30 Apr 2022 4 x 2053 ml 3-chamber infusion bag 22 Sep 2020
10PM9641 30 Nov 2022 4 x 2053 ml 3-chamber infusion bag 20 Apr 2021
10QA1922 31 Dec 2022 4 x 2053 ml 3-chamber infusion bag 23 Apr 2021
10QD5451 31 Mar 2023 4 x 2053 ml 3-chamber infusion bag 04 Oct 2021
10QH8524 31 Jul 2023 4 x 2053 ml 3-chamber infusion bag 06 Jan 2021

Active Pharmaceutical Ingredients: Purified soyabean oil, glucose monohydrate, alanine, arginine, aspartic acid, glutamic acid, glycine, histidine, isoleucine, leucine, lysine hydrochloride, methionine, phenylalanine, proline, serine, taurine, threonine, tryptophan, tyrosine, valine, calcium chloride (as dihydrate), sodium glycerophosphate (as hydrated), magnesium sulphate (as heptahydrate) potassium chloride, sodium acetate (as trihydrate).

Brief description of the problem

Fresenius Kabi Limited have identified an error in the infusion the infusion bag packaged into the above batches. In the list of ingredients section printed onto the bag, the amount of Glucose 19 %: Glucose (monohydrate) has been incorrectly declared as 110 g, the actual amount is 220 g.

The correct amount of carbohydrates (as glucose anhydrous) is correctly declared on the infusion bag within the energy content section as 200 g. The correct amounts are also stated on the outer carton and in the SmPC.

All other Kabiven bag sizes state the correct amount of glucose in both monohydrate and anhydrous form.

A photograph in the attachment shows an infusion bag with the error. On the left-hand side of the photograph circled in red in the correctly declared amount of glucose anhydrous, 200 g, and on the right-hand side of the
photograph also circled in red is the incorrectly declared amount of glucose monohydrate, 110 g.

Advice for healthcare professionals

There is no risk to product quality as a result of this issue, therefore the affected batches are not being
recalled. Healthcare professionals are advised to exercise caution when administering this product
particularly when calculating patient nutritional requirements.

Fresenius Kabi Limited have confirmed that all future batches will contain an infusion bag with the correct
declaration of the amount of glucose monohydrate and equivalent glucose anhydrous.

Further Information

For more information or medical information queries please contact:
Medical.Information-UK@fresenius-kabi.com

Recipients of this Medicines Notification should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to community pharmacists and dispensing general practitioners for information.

Download the document

Class 4 Medicines Defect Information: Fresenius Kabi Limited, Kabiven Emulsion for Infusion, EL (22)A/02

Updated 25 January 2022. This page summarises an official notice. Details can change – always follow the official notice.

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