9 FDA recalls mention Carbidopa. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Carbidopa.
Reason Product mix up: complaint received that sealed medication bottle contained Carbidopa, Levodopa, and Entacapone film-coated tablets (37.5 mg/150…
Reason Packaging defect: observed packaging defect, blister packaging inadequately sealed.
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Reason Product Mix-Up: A foreign tablet was found in bottle.
Reason Failed Stability Specifications: confirmed out of specification results obtained during refrigerated material stability testing indicating that drug…
Reason Failed Dissolution Specifications
Reason Failed Tablet/Capsule Specifications: Teva is recalling one lot of Carbidopa and Levodopa Tablets USP, 25mg/100mg due to the potential for…
Reason Chemical Contamination: Novartis Pharmaceuticals Corporation has recalled physician sample bottles of Diovan, Exforge, Exforge HCT,Lescol XL…
Reason Labeling: Label Mixup: CARBIDOPA/LEVODOPA, Tablet, 25 mg/250 mg may have potentially been mislabeled as the following drug: DIGOXIN, Tablet, 0.125…
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