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Last updated: 2022
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Recall class: Type III
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- (-) 2022
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Displaying 1 - 15 of 17 items.
The concentration of the medicinal ingredient, sodium fluoride, is out of specification in the affected lot.
RecallHealth product recall | 2022-12-15
Product sterility may be compromised in the affected lot.
RecallHealth product recall | 2022-12-14
Affected lot has incorrect product image on the product label.
RecallHealth product recall | 2022-11-21
The potency of the medicinal ingredient (Vitamin C) is out of specification in the affected lot(s).
RecallHealth product recall | 2022-10-07
The product lot did not meet product specification at end of shelf life.
RecallHealth product recall | 2022-09-02
Product not manufactured to product specifications/licence and does not contain the required risk information.
RecallHealth product recall | 2022-08-19
Package insert missing French instructions.
RecallHealth product recall | 2022-07-14
Affected lot contain sodium chlorite levels outside of the labelled claim.
RecallHealth product recall | 2022-07-14
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
Affected lots may contain active ingredients that are above the labelled dosage.
RecallHealth product recall | 2022-05-20
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 affected lot may contain Bio-Calcium D tablets.
RecallHealth product recall | 2022-05-02
The lot number and/or expiration date may not appear on the affected lot label.
RecallHealth product recall | 2022-04-06