Labelling error reported for Ponlimsi pre-filled syringes

Teva UK Limited is reporting a labelling error on the carton for Ponlimsi (Denosumab) 60mg Solution for injection in Pre-filled Syringe. The carton states “For application to the skin” when the product is licensed for subcutaneous use.

From: Medicines and Healthcare products Regulatory Agency

Published 4 June 2026

Message type: Medicines recall/notification

Medical specialty: Dispensing GP practices and General practice

Issued: 4 June 2026

DMRC reference number

DMRC - 39320587

Marketing Authorisation Holder

Teva UK Ltd

Medicine Details

Ponlimsi (Denosumab) 60mg Solution for Injection in Pre-filled Syringe

PL: 00289/2645

Active Ingredient: denosumab

SNOMED code: 45668211000001103

GTIN: 5017007608233

Affected Lot Batch Numbers

Batch No. Expiry Date Pack Size First Distributed

184472 30/11/2028 1 pre-filled syringe 21/01/2026

186711 30/11/2028 1 pre-filled syringe 21/04/2026

188656 28/02/2029 1 pre-filled syringe 01/06/2026

Background

Teva UK Limited is reporting a labelling error on the carton for Ponlimsi (Denosumab) 60mg Solution for injection in Pre-filled Syringe.  The carton states “For application to the skin” when the product is licensed for subcutaneous use.

This notification contains batches that have commenced distribution  from 21/01/2026 onwards. All 3 batches have been manufactured and packed with the erroneous carton, however as the product administration should be performed by an individual who has been adequately trained in injection techniques, these batches will not be repackaged and continue to be distributed. Teva UK Limited have confirmed that all future deliveries will be supplied with a copy of this notification to help remind healthcare professionals and patients that this product is for subcutaneous use.

This error is circled in red on the image below:

Advice for Healthcare Professionals:

There is no risk to product quality as a result of this labelling error. Aside from the labelling error, no additional errors have been identified with the product or delivery device, therefore the affected batches are not being recalled.

Healthcare professionals are advised to reassure patients, if contacted, that the product is for subcutaneous injection as described in the Patient Information Leaflet, which contain clear instructions for intended use.

The Summary of Product Characteristics and Patient Information Leaflet can be accessed at the following website https://products.tevauk.com/hcp/denosumab-823?productId=27077

Advice for Patients:

Patients should continue to use syringes from these batches as prescribed by your healthcare professional. This does not affect the quality of the medicine. The cartons contain a syringe for subcutaneous injection as prescribed, and this is a labelling error.

If you have concerns about a medicine you may be using, please contact your healthcare professional.

Patients who experience adverse reactions or have any questions about their medication should seek medical attention. Any suspected adverse reactions should also be reported via the MHRA Yellow Card scheme.

Additional information:

For all medical information enquiries and information on this product, please email medinfo@tevauk.com

For stock control enquiries please email Customer.services@tevauk.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.

Yours faithfully

Defective Medicines Report Centre

10 South Colonnade

Canary Wharf

London

E14 4PU

Telephone +44 (0)20 3080 6574

DMRC@mhra.gov.uk

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Class 4 Medicines Defect Notification: Teva UK Ltd, Ponlimsi (Denosumab) 60mg Solution for Injection in Pre-filled Syringe, EL(26)A/27

Updates to this page

Published 4 June 2026

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