▣ ScanRecallsGet the app ↗

OFFICIAL-SOURCE RECALL · UNITED KINGDOM

Class 4 Medicines Defect Notification: Teva UK Ltd, Ponlimsi Recall: Teva UK Limited is reporting a

Use the identifiers printed on your item to determine whether this recall may affect the product you own.

CountryUnited KingdomPublishedJune 4, 2026Last updatedJune 4, 2026Official source last checkedSeptember 9, 2026 at 1:48 PM UTC

CHECK THE ITEM YOU OWN

Is your product affected?

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

The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.

Why this product was recalled

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.

Hazard

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.

What consumers should do

for Healthcare Professionals: There is no

Official recall notice

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

Agency: Medicines and Healthcare products Regulatory Agency

Official publication date: June 4, 2026

Read the official UK_MHRA recall notice →

SCAN ONCE. KEEP WATCHING.

Keep an eye on the products at home.

Scan food and household product barcodes, save your items and get notified when a future recall may match.

Download on the App StoreGet it on Google Play

Browse connected recall information

Related recalls

Download on the App StoreGet it on Google Play