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Recall class

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Displaying 1 - 15 of 530 items.

" " Allergenic Extract Non Pollens (Pecan Nut): False negative for skin test
 Affected lot may result in a false negative for skin test (pecan nut allergy)
RecallHealth product recall | 2023-09-29
" " ATROPINE SULFATE INJECTION USP: Affected lot may contain the presence of glass particulate.
 Affected lot may contain the presence of glass particulate.
RecallHealth product recall | 2023-09-20
" " Chlordiazepoxide: Affected lot may be OOS
Affected lot may be OOS for related compound CZ RC1
RecallHealth product recall | 2023-09-19
" " ELIGARD 7.5mg: may not be filled with correct amount of leuprolide acetate.
Affected lot may not be filled with the correct amount of leuprolide acetate.
RecallHealth product recall | 2023-09-12
" " Allergenic Extract Non Pollens: False negative for skin test
 Affected lot may result in a false negative for skin test (pecan nut allergy)
RecallHealth product recall | 2023-09-07
" " CEQUA: Out of Specification
The stability assay is out of specification in the affected lots.
RecallHealth product recall | 2023-09-06
" " Stiff Rock: Affected lots may contain the undeclared ingredients sildenafil and tadalafil
Affected lots may contain the undeclared ingredients sildenafil and tadalafil.
RecallHealth product recall | 2023-08-23
" " Pink Unicorn: Affected lots may contain the undeclared ingredient sildenafil (updated risk classification and reason for recall)
Affected lots may contain the undeclared ingredient sildenafil.
RecallHealth product recall | 2023-08-22
" " Micafungin Sodium for Injection 50 mg/vial and 100 mg/vial: Linear barcode printed on the vial label is non-functioning
Linear barcode printed on the vial label is non-functioning.
RecallHealth product recall | 2023-08-21
" " Multi-Peptide Lash Serum: undeclared ingredient and sold without market authorization
Affected lots contain an undeclared ingredient (bimatoprost). Product sold without market authorization (DIN) in Canada.
RecallHealth product recall | 2023-08-21
" " FEG Eyelash Enhancer: Unauthorized Product with ingredient on prescription drug list.
Product sold without market authorization (DIN) in Canada. Product contains undeclared ingredient, bimatoprost, that is listed on the prescription drug list 
RecallHealth product recall | 2023-08-18
" " PMS-AMITRIPTYLINE 10 mg, 25 mg, and 50 mg: NDMA and NNORT impurity
Affected lots exceed the interim acceptable intake limit for N-nitroso-nortriptyline (NNORT) or exceed the acceptable cumulative intake limit for (N-nitrosodimethylamine (NDMA) and NNORT).
RecallHealth product recall | 2023-08-16
" " AMITRIPTYLINE 10 & 50mg: NDMA and NNORT impurity
Affected lot exceed  the acceptable cumulative intake limit for N-nitrosodimethylamine (NDMA) and N-nitroso-nortriptyline (NNORT).
RecallHealth product recall | 2023-08-16
" " Apo-Acyclovir Tablets: NDMA impurity (Updated with new product and lot numbers)
Affected lot exceeds concentration limit for N-nitrosodimethylamine (NDMA).
RecallHealth product recall | 2023-08-14
" " APO-AMITRIPTYLINE Tablets: NNORT impurity
Affected lots exceed the interim acceptable intake limit for N-nitroso-nortriptyline (NNORT).
RecallHealth product recall | 2023-08-14
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