Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,616 recalls have been distributed to District of Columbia in the last 12 months.
Showing 7401–7420 of 13,355 recalls
Recalled Item: Divalproex Sodium Delayed Release Tablets USP Recalled by Unichem...
The Issue: Cross Contamination With Other Products: metronidazole powder was found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Oral Solution Recalled by Akorn Inc Due to CGMP Deviations:...
The Issue: CGMP Deviations: Inadvertent release of a drug product with unapproved...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.25% Acetic Acid Irrigation USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: identified as polyethylene, which is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Amneal Pharmaceuticals Due to...
The Issue: Presence of particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP Recalled by...
The Issue: Failed Impurities/Degradation Specifications: High out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ Recalled...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion (zinc oxide 23.8%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Luxurious Eye & Lip Collection contains Recalled...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL)...
The Issue: Failed Stability Specifications: Product stability testing results did not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Auryxia (ferric citrate) tablets Recalled by Keryx Biopharmaceuticals, Inc....
The Issue: Presence of Foreign Substance: Reports have been received of damaged...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - product label was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena deep clean purifying whipped foam cleanser Recalled by Johnson &...
The Issue: Defective Container: products showed leakage (bubbles, foaming) of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Acne Proofing whipped foam cleanser Recalled by Johnson & Johnson...
The Issue: Defective Container: products showed leakage (bubbles, foaming) of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean...
The Issue: Defective Container: products showed leakage (bubbles, foaming) of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BodySlim Herbal Advanced technology & Strong formula capsules Recalled by...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.