Teva Pharmaceuticals USA recalls Tretinoin Capsules, 10 mg, 100 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0555-0808-02
Failed Dissolution Specifications; Low Out of specification (OOS) results for dissolution.
Read the official notice →- Date
- 2022-02-09
- Country
- United States
- Brand
- Teva Pharmaceuticals
- Product
- Tretinoin Capsules, 10 mg, 100 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0555-0808-02
- Classification
- Class II
- Units
- nationwide in the USA
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Teva Pharmaceuticals recalls
- 2022-05-04
US
- 2022-04-20
US
Teva Pharmaceuticals USA Inc recalls IDArubicin Hydrochloride Injection USP 5gm/5mL (1mg/mL) for intravenous use, 5mL Single Dose Vial, Rx Only, Teva Pharmaceuticals,…
Presence of Particulate Matter: Product was found to contain silica and iron oxide
- 2022-02-09
US
US
Teva Pharmaceuticals USA recalls Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10 mg/10 mg, 100-count bottle, Rx Only, Manufactured by:…
Failed Dissolution Specification: Dissolution results are below specification limits for the active ingredient
- 2022-01-26
US
Teva Pharmaceuticals USA recalls Brinzolamide Ophthalmic Suspension, USP 1%, packaged as a)10 ml dropper bottles (NDC 0591-2127-79), and b) 15 ml dropper bottles (NDC…
Defective Container: The notch in the cap that fits into the nozzle of the dropper could break off and block the dropper possibly resulting in the product not dispensing.
- 2022-01-19
US
Teva Pharmaceuticals USA recalls MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only, Manufactured for:…
Lack of Assurance of Sterility
FDA · DrugTeva Pharmaceuticals USAMethylprednisolone, TN Norepinephrine BItartrate - MS, OHOfficial notice →
Other drugs & medical recalls in the United States
- 2022-02-09
US
Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion Pumps, Product code 3570009.
There is the potential for reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of incorrect administration set setup and/or incomplete resolution of…
FDA · DeviceBaxter Healthcare CorporationWorldwide Distribution. US nationwide Puerto Rico and St. Thomas. There was…Official notice →US
Empowered Diagnostics LLC recalls CovClear COVID-19 Rapid Antigen Test, ATG 900-031
COVID test kits were offered for sale and distributed to consumers in the United States without marketing approval, clearance, or authorization from FDA.
US
US
US
US
Teva Pharmaceuticals USA recalls Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10 mg/10 mg, 100-count bottle, Rx Only, Manufactured by:…
Failed Dissolution Specification: Dissolution results are below specification limits for the active ingredient