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.

Class 2 Recall on Various Children’s Dry Cough Meds

Bell, Sons & Co is recalling 15 batches of the cough syrups listed above to patient-level as a precautionary measure due to a small number of reports of mould.

Class 4 Drug Alert (Caution in use) Bleo-Kyowa Powder For Sol For Inj 15,000iu

Kyowa Kirin is advising caution in use for one lot of Bleo-Kyowa, Powder for Solution for Injection, 15,000 IU following the detection of glass particles.

Field Safety Notice on Medset CM Breast Pump Kit

Medela AG found that labelling documentation for the Medset CM Breast Pump Kit is incomplete. Additionally, although all product is sterile, we cannot demonstrate full compliance with the quality...

Company-Led Drug Alert on Phenytoin 90mg/5ml Oral Suspension

Rosemont Pharmaceuticals Ltd is recalling the below batches to Pharmacy Level as a precaution due to the generation of data which indicates that the product becomes difficult to resuspend over shelf...

Field Safety Notice on Accu-Chek Aviva & Performa Test Strips

Roche have identified certain test strips lots that potentially show an increase in strip errors prior dosing. Due to the designed fail-safe in the blood glucose meter, the issue can be identified by...

Class 3 Recall on Latanoprost/Timolol Eye drops

FDC Pharma are recalling the below batch due to an out of specification result for an unknown impurity during stability testing.
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