Brand Recall Hub
Dose Recalls in Canada
27 recalls found for Dose. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.
27 Dose Recalls
Enteric Coated Daily Low Dose ASA 81mg: free salicylic acid can be out of specification
Product quality
View recall details →
CISATRACURIUM BESYLATE INJECTION USP MULTIDOSE: The level of the degradation product Benzaldehyde is out of specification in the affected lots.
Product quality
View recall details →
All lots of JAMP-Clopidogrel 75 mg and AG-Clopidogrel 75 mg tablets recalled due to possible incorrect dose, which may pose health risks
Product safety - Dosage
View recall details →
Importation of US-authorized Epinephrine Injection USP, 1 mg/10 mL Single-Dose Pre-Filled Syringes Due to the Current Shortage of Canadian-Authorized Epinephrine Injection USP, 1 mg/10 mL Single-Use Syringes
Supply - Dosage - Packaging
View recall details →
All lots of JAMP-Mycophenolate 250 mg capsules recalled due to possible incorrect dose, which may pose health risks
Product safety
View recall details →
JAMP Digoxin 0.0625 mg and 0.125 mg tablets recalled due to possible incorrect dose, which may pose health risks
Product safety
View recall details →
JAMP Digoxin tablets: One lot recalled due to possible oversized tablets which may pose overdose risk
Product safety
View recall details →
Hydrasense Baby Nasal Care Easydose
Sterility
View recall details →
JAMP TELMISARTAN-HCT: Affected lots may contain higher dosage than the labelled dose
Product quality
View recall details →
Pediatrix Acetaminophen Oral Solution for children: One lot recalled due to potential risk of overdose
Product safety
View recall details →
Certain bottles of JAMP Venlafaxine XR 37.5 mg capsules recalled due to mislabelling that could lead to overdose
Labelling
View recall details →
Dose IQ Safety Software
Performance
View recall details →
PMS-Hydromorphone: Affected lot may contain tablets that could potentially lead to overdose
Adverse reaction - Dosage - Labelling - Packaging - Product safety - Product withdrawal
View recall details →
Recall of one lot of pms-Hydromorphone due to packaging error that could potentially lead to overdose
Adverse reaction - Dosage - Labelling - Packaging - Product safety - Product withdrawal
View recall details →
Distribution of a New Presentation of SPIKEVAX (elasomeran) COVID-19 Vaccine (0.10 mg/mL in 2.5 mL multidose vial) with English-only Vial and Carton Labels
Labelling - Packaging - Product safety - COVID
View recall details →
Spectrum Iq Infusion System With Dose Iq Safety Software
Performance
View recall details →
Two lots of Novo-Gesic Forte/Acetaminophen recalled due to labelling error that may lead to overdose and in the most severe cases, death
View recall details →
Spectrum IQ Infusion System with Dose IQ Safety Software (2021-06-10)
Medical devices
View recall details →
Importation of COVID-19 Vaccine Moderna with up to 15 Doses per Vial and English-only Vial and Carton Labels (US-Labelled Supply)
Labelling - New safety information - Packaging - Supply - COVID
View recall details →
Spectrum IQ Infusion System with Dose IQ Safety Software (2021-03-17)
COVID - Medical devices
View recall details →
Important Safety Information on SUBOXONE (buprenorphine and naloxone) and the Risk of Overdose or Underdose when Switching Between Dosage Forms or Routes of Administration
Product safety
View recall details →
Spectrum IQ Infusion System with Dose IQ Safety Software (2020-11-26)
Medical devices
View recall details →
Spectrum IQ Infusion System with Dose IQ Safety Software (2020-09-04)
Medical devices
View recall details →
Three lots of antidiuretic DDAVP Spray recalled because of potential overdose risk
View recall details →
Cisatracurium Omega Multi-Dose (Cisatracurium Besylate Injection): Temporary change of ferrule (metal seal) colour to maintain continued supply in Canada
Product safety
View recall details →
PropoVet Multidose 10mg/ml (2018-06-18)
Product safety
View recall details →
Ventolin Diskus: One lot recalled as inhalers may not deliver the intended dose
View recall details →