FDA
Vitality: Vitality male enhancement dietary supplement capsules
Undeclared Sildenafil and Tadalafil
- Recall
Medicine recalls
The name on the prescription is only part of the check. Manufacturer, strength and lot determine which medicine a notice covers. Your pharmacist can help identify what you received.
- Indexed notices
- 179
- Primary sources
- FDA
What this category covers
Prescription medicines, Over-the-counter medicines, Eye drops, Sunscreens. Prescription and over-the-counter medicines. Identify the affected product and follow FDA’s notice.
Check with the official agency or read the product identification guide. Source coverage explains which notices are indexed and when each source was imported.
Recalls & safety alerts
179 indexed notices. Always compare with the current official notice.
FDA
BD: ChloraPrep Clear 1 mL applicator skin preparation product
Potential for fungal contamination under certain environmental conditions allowing the growth of Aspergillus penicillioides
- Recall
FDA
ICU Medical: POTASSIUM CHLORIDE Inj. 20 mEq and 10 mEq
Bags of POTASSIUM CHLORIDE Inj. 20 mEq have incorrect overwrap labels which state POTASSIUM CHLORIDE Inj. 10 mEq.
- Recall
FDA
Alvogen: Fentanyl Transdermal System 25 mcg/h transdermal patches
There is potential that patches could be multi-stacked, adhered one on top of the other, in a single product pouch
- Recall
FDA
Provepharm Inc.: Phenylephrine hydrochloride Injection, USP, 10 mg/ mL
Device & Drug Safety – Potential Foreign Material
- Recall
- Recall
- Recall
FDA
Par Pharmaceutical: Adrenalin® Chloride Solution (EPINEPHrine nasal solution, USP)
Product is an unapproved drug.
- Recall
Read the product identification guide
Official checking resources
- FDA drug recalls — Official drug recall announcements and additional recall resources.
- Understand a medicine recall — FDA guidance on checking lots and next steps for patients.
Data sources & coverage
Official sources may have newer notices or a broader history. See all sources and coverage.