Class II · Moderate risk Terminated
Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc…
Reason Subpotent Drug.
Is Etomidate recalled?
5 FDA recalls mention Etomidate. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Etomidate.
Class III · Low risk Ongoing
Amidate (Etomidate Injection, USP), 40 mg/20 mL (2 mg/mL), LifeShield, 20 mL, Glass Abboject Syringe with male luer lock adapter…
Reason Failed Impurities/Degradation Specifications: Out of Specification(OOS) results for degradation product of etomidate was confirmed during stability…
Class II · Moderate risk Terminated
Etomidate active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front…
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
Class II · Moderate risk Terminated
etomidate injection, USP, 2 mg/mL, packaged in a) 20 mg/10 mL (2 mg/mL), 10 mL Single Dose Vials (NDC 0069-0006-02), 10 x 10 mL…
Reason Presence of Particulate Matter: Potential for small black particles to be present in individual vials, the potential for missing lot number and/or…
Class II · Moderate risk Terminated
ETOMIDATE 0.2% (2MG/ML) INJECTABLE 20 ML (1 PRODUCT)
Reason Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because…
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