RecallReported September 2, 2026
Class II recall by Hikma Pharmaceuticals USA INC.
Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05) bottles, Rx only, Manufa…
FDA's enforcement report of September 2, 2026 lists a Class II recall by Hikma Pharmaceuticals USA INC. of Columbus, OH. Product: Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05) bottles, Rx only, Manufa…. Status: Ongoing.
On the record
- Recalling firm
- Hikma Pharmaceuticals USA INC.
- Location
- Columbus, OH
- Classification
- Class II
- Status
- Ongoing
- Recall number
- D-0831-2026
- Product type
- Drugs
- Brand names
- RAMIPRIL
- Generic names
- RAMIPRIL
- Recall initiated
- 2026-08-24
- Reported by FDA
- 2026-09-02
The full record
An account shows the reason for the recall, where the product was distributed and the lots.
What a recall is
FDA classifies a recall by the hazard. Class I: a reasonable probability that the product will cause serious adverse health consequences or death. Class II: the product may cause temporary or medically reversible harm, or the probability of serious harm is remote. Class III: the product is not likely to cause adverse health consequences.
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From FDA enforcement reports. The record may have changed since it was read.
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