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Last updated: 2024
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Displaying 1 - 15 of 27 items.
TEVA-ECTOSONE: Presence of contaminant (degradant) in affected lot.
RecallHealth product recall | 2024-06-21
Dianeal PD4 2.5% Dextrose and Physioneal 40 2.27% Glucose peritoneal dialysis solutions recalled due to risk of leakage at connection site
RecallHealth product recall | 2024-06-14
PMS-PIRFENIDONE 267 & 801 mg: Data integrity concerns with products bioequivalence data that could lead to incorrect dosing.
RecallHealth product recall | 2024-06-07
Mint-Betahistine 8, 16 & 24mg: Data integrity concerns with product's bioequivalence data that could lead to incorrect dosing.
RecallHealth product recall | 2024-06-06
Accel-Ondansetron ODT 4 & 8 mg: Data integrity concerns with product's bioequivalence data that could lead to incorrect dosing.
RecallHealth product recall | 2024-06-06
Jamp Digoxin tablet: Over-sized tablet
RecallHealth product recall | 2024-06-03
Octaplasma solution: exposed to temperatures outside of the recommended storage conditions
RecallHealth product recall | 2024-06-03
Probiotic antibiotic support capsule: Out-of-specification (Bacterial content)
RecallHealth product recall | 2024-05-27
Tisseel Kit; Out-of-specification (Dissolution)
RecallHealth product recall | 2024-05-23
Sanis Health Duloxetine 60 mg Capsule; Exceeds acceptable interim intake limit for N-nitroso-duloxetine (NDLX)
RecallHealth product recall | 2024-05-16
Sandoz Fesoterodine Fumarate 8 mg tablet; Out-of-specification (diester impurity)
RecallHealth product recall | 2024-05-16
REDDY-SAPROPTERIN: Color change & decrease potency
RecallHealth product recall | 2024-05-03
PMS-Duloxetine 60 mg: Exceeds acceptable interim intake limit for N-nitroso-duloxetine (NDLX)
RecallHealth product recall | 2024-04-17
PMS-Duloxetine 30 mg: Exceeds acceptable interim intake limit for N-nitroso-duloxetine (NDLX)
RecallHealth product recall | 2024-04-17
I-131 Diagnostic Capsule: Affected lots may have decreased thyroid uptake.
RecallHealth product recall | 2024-04-17