Class III · Low risk
Carisoprodol Tablets
Failed Impurity/degradation Specification
Is Carisoprodol recalled?
Not under an active recall.
Carisoprodol was recalled 6 times in the past — all now closed. Most recent: Jan 28, 2014.
Most common reason: Particulate / foreign matter (4 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Carisoprodol. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Carisoprodol recalls on record
none so far in 2026; 6 on record, newest first
Class II · Moderate risk
Carisoprodol Tablets
Presence of Foreign Substance; metal particulates were visually observed in the tablets.
Class II · Moderate risk
Carisoprodol IV
Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inactive components of the product were visually observed during routine stability testing.
Class II · Moderate risk
Carisoprodol Tablets
Presence of Foreign Substance; heavy metals (chromium, titanium etc) and inactive components of the product were visually observed during routine stability testing
Class II · Moderate risk
Carisoprodol Tablets
Presence of Foreign Substance: Uncharacteristic blacks spots on tablets.
Class III · Low risk
Carisoprodol Tablets
Labeling: Not elsewhere classified: On 12/12/11, DEA published a final rule in the Federal Register making this product a schedule IV (C-IV)controlled substance. This product is being recalled because this controlled product was not relabeled with the required "C-IV" imprint on the label for products distributed after the 06/11/12 deadline.
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