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Recall class: Type III
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Displaying 1 - 15 of 98 items.
Affected lots may be missing the DIN and Canadian contact information on the outer label.
RecallHealth product recall | 2023-05-05
The Loss on Drying is out of specification in the affected lot.
RecallHealth product recall | 2023-03-21
Product sterility may be compromised in the affected lot.
RecallHealth product recall | 2022-12-14
Potential for a future out of specification result during shelf-life
RecallHealth product recall | 2022-09-28
Out of specification result for assay test in the affected lots
RecallHealth product recall | 2022-08-31
Affected cylinders may not be filled with adequate amount of product.
RecallHealth product recall | 2022-07-13
Product sold without market authorization. Affected lots are labelled with unauthorized claims.
RecallHealth product recall | 2022-06-30
The Benzalkonium Chloride assay is out of specification in the affected lot.
RecallHealth product recall | 2022-06-23
Presence of one (1) AA-FENO-SUPER 100 mg tablet in affected lot of AA-FENO-SUPER 160 mg.
RecallHealth product recall | 2022-05-05
The Vial 1 assay may be out of specification in the affected lot(s).
RecallHealth product recall | 2022-03-24
The product lots may not meet product specification at end of shelf life.
RecallHealth product recall | 2022-03-02
The assay is out of specification in the affected lot
RecallHealth product recall | 2022-02-23
The dissolution is out of specification in the affected lot(s).
RecallHealth product recall | 2022-01-31
Vita Health Ibuprofen product recall (2021-10-01)
Starting date:
October 1, 2021
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type III
Source…
RecallHealth product recall | 2021-10-01
TARO-Bupropion XL (2021-09-13)
Starting date:
September 13, 2021
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type III
Source of recall:
Health…
RecallHealth product recall | 2021-09-13