Progesterone Injection USP
Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.
Cause type: Labeling / mix-up
Wrong label, wrong strength, mixed-up products, or packaging errors. One of the most dangerous causes - you can end up taking the wrong drug or the wrong dose. All labeling / mix-up recalls.
Progesterone E4M SR 100 mg capsules
Drug: Progesterone
Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.
Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
Presence of Foreign Substance; Broken metal piece found embedded in tablet.
cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.
Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.
Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.
Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.
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