Class 2 Recall on Ozurdex 700 micrograms intravitreal implant in applicator

Allergan Pharmaceuticals Ireland is recalling the below batches due to the possibility that a single loose silicone particle of approximately 300microns in diameter may become detached from the needle...

Company Led Drug Alert on Imatinib 400mg Capsules (3 x 10)

Cipla (EU) Limited has informed MHRA that there is an error on the Patient Information Leaflet (PIL) for the below product: the dosage information for the indication CML is incorrect..

Class 4 Drug Alert (Caution in Use) on Caspofungin 70mg powder

Cadiasun Pharma GmBH has informed us that there is an error on the patient information leaflet for the below product.

Class 4 Drug Alert (Caution in Use) on Olmetec 20mg Film-Coated Tablets

Daiichi Sankyo UK Limited has informed us that there is an error on the blister foil of the above batches of Olmetec 20mg Film-Coated Tablets.

Field Safety Notice on CoaguChek

Roche Diagnostics has issued a Field Safety Notice on the batches below due to an increase in complaints regarding deviations against laboratory methods during the last weeks. Therefore, Roche...

Company Led Drug Alert on Nutriflex Omega & Nutriflex Lipid 2500ml

B. Braun Medical Ltd are recalling specific batches of Nutriflex Omega Special 2500ml and Nutriflex Lipid Special without Electrolytes 2500ml as it's been identified that they may have an out of...

Company-Led Drug Alert on Melatonin Cap 10mg

IPS Specials are recalling specific batches of Melatonin 10mg capsules because they have been assigned an incorrect extended expiry date.

Class 1 Recall on Valsartan

Dexcel Pharma Ltd and Actavis Group PTC (now Accord) are recalling all batches of Valsartan due to contamination.

Class 2 Recall on Fiasp Flextouch 100u/Ml

Novo Nordisk received a customer complaint from UK related to Fiasp, batch was examined microscopically and found to be out of specification (OOS) as particles were detected in insulin.

Class 2 Recall on Denzapine 50mg/Ml Oral Suspension

Britannia Pharmaceuticals Ltd is recalling the below batches because of increased crystallisation of the active ingredient which may affect delivery of the full dose.
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