Browse Drug Recalls
5 FDA drug safety recalls.
FDA Drug Recall Enforcement Database
Browse 5 FDA drug recall enforcement actions. Each entry includes the product description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.
Drug Safety Recalls
Browse 5 FDA drug recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Dec 14, 2017 | Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ (octinoxate... | GMP Deviations: manufacturing of API material did not meet GMP and quality requirements. | Class II | SHISEIDO AMERICA INC. |
| Dec 14, 2017 | Shiseido Future Solution LX Luxurious Eye & Lip Collection contains SPF 50+ (... | GMP Deviations: manufacturing of API material did not meet GMP and quality requirements. | Class II | SHISEIDO AMERICA INC. |
| Dec 14, 2017 | bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion (zinc oxide 23.8%, titan... | GMP Deviations: manufacturing of API material did not meet GMP and quality requirements. | Class II | SHISEIDO AMERICA INC. |
| Dec 14, 2017 | Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%, ... | GMP Deviations: manufacturing of API material did not meet GMP and quality requirements. | Class II | SHISEIDO AMERICA INC. |
| Dec 14, 2017 | Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%, octoc... | GMP Deviations: manufacturing of API material did not meet GMP and quality requirements. | Class II | SHISEIDO AMERICA INC. |
Frequently Asked Questions
When a drug safety issue is identified — through FDA inspections, laboratory testing, adverse event reports, or manufacturer quality checks — the responsible company issues a recall to remove the affected products from the market. Pharmacies pull the product from shelves, and consumers are advised to contact their healthcare provider for alternatives.
The leading causes include cGMP deviations, impurity contamination (including nitrosamines like NDMA), failed dissolution or stability testing, sterility issues, potency problems, labeling errors, and foreign particle contamination.
Use the search and filter tools on this page to look up specific medications, active ingredients, or manufacturers. Each recall entry includes the product description, lot numbers, and distribution details.