Carisoprodol Tablets, USP, 350 mg, unit dose blister packages of 100 tablets (10 cards of 10 tablets each), Rx only, Manufactured…
Reason Failed Impurity/degradation Specification
6 FDA recalls mention Carisoprodol. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Carisoprodol.
Reason Failed Impurity/degradation Specification
Reason Presence of Foreign Substance; metal particulates were visually observed in the tablets.
Reason Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inactive components of the product were visually observed during routine…
Reason Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inactive components of the product were visually observed during routine…
Reason Presence of Foreign Substance: Uncharacteristic blacks spots on tablets.
Reason Labeling: Not elsewhere classified: On 12/12/11, DEA published a final rule in the Federal Register making this product a schedule IV…
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