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Last updated: March 2022
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Last updated: 2022
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Displaying 1 - 13 of 13 items.
The Vial 1 assay may be out of specification in the affected lot(s).
RecallHealth product recall | 2022-03-24
UPDATED INFORMATION – May 6, 2022
Further to the communication below, issued on March 15, 2022, regarding the potential for the presence of particulate matter in vials of Sodium Acetate Injection, USP (DIN 02139529) from lot 6126554, Fresenius Kabi…
AlertHealth professional risk communication | 2022-03-15
Presence of N-nitrosodimethylamine (NDMA) close or above the acceptable concentration limit in affected lots.
RecallHealth product recall | 2022-03-11
UPDATE: March 11, 2022 – Pharmascience Inc. recalls 30 lots of 150 mg over-the-counter ranitidine packaged in blister packs
Pharmascience Inc. is recalling 30 lots of over-the-counter ranitidine drugs (150 mg tablets), packaged in blister packs, after…
AlertInformation update | 2022-03-11
UPDATED INFORMATION – March 10, 2022
Further to the Health Canada communication below, issued on June 15, 2021, while initial estimates of supply and demand forecasted that the global shortage could impact Canada’s supply in early 2022, careful…
AlertHealth professional risk communication | 2022-03-10
Intravenous bags of Baxter’s 0.9% Sodium Chloride Injection, USP 500 mL and Lactated Ringer’s Injection, USP 500 mL from certain lots have the potential to leak when administered under pressure infusion due to a weak seal formation.
Affected lots are…
AlertHealth professional risk communication | 2022-03-09
Unspecified impurities are out of specification in the affected lot.
RecallHealth product recall | 2022-03-08
Intravenous bag may be leaking in affected lot
RecallHealth product recall | 2022-03-07
Presence of particulate matter in affected lots.
RecallHealth product recall | 2022-03-07
Presence of impurity N-Nitroso-quinapril above the acceptable concentration limit in affected lots.
RecallHealth product recall | 2022-03-04
The product lots may not meet product specification at end of shelf life.
RecallHealth product recall | 2022-03-02
Presence of impurity N-Nitroso-propanolol above the acceptable concentration limit in affected lots.
RecallHealth product recall | 2022-03-02
Pfizer Canada ULC is recalling all lots of Inderal-LA (propranolol hydrochloride) extended release capsules, in 60 mg, 80 mg, 120 mg and 160 mg strengths, due to the presence of a nitrosamine impurity (N-nitroso-propranolol) above the acceptable level…
AlertPublic advisory | 2022-03-01