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. 2,552 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16001–16020 of 47,654 recalls
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for mechanical peel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01...
The Issue: Crystallization: customer complaints for crystallization in finished product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01...
The Issue: Crystallization: customer complaints for crystallization in finished product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ferrara Candy Company assorted candy Heart Box Recalled by Ferrara Candy...
The Issue: Undeclared ingredients on retail packaging, including but not limited to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray Recalled by...
The Issue: The product may be contaminated with Burkholderia cepacia
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC...
The Issue: Potential total iron-binding capacity (TIBC) results. The VITROS TIBC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct...
The Issue: Teleflex is voluntarily recalling the products above due to customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methacholine Challenge 5-Syringe Test Kits Recalled by Edge Pharma, LLC Due...
The Issue: Temperature Abuse; labeled with the incorrect room temperature (15-25 ¿C)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imatinib Mesylate Tablets 100mg Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MedSchenker Smart Transport Medium (STM) System: CULTURE MEDIA Recalled by...
The Issue: Discoloration and turbidity were present in the specified lots of STMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for Recalled by...
The Issue: Contact lenses may be mislabeled with the incorrect lens power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adam's Secret Extra Strength 1500 Recalled by Adams.Secret.co Due to...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adam's Secret Extra Strength 3000 Recalled by Adams.Secret.co Due to...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Chemical contamination; Unknown brown residue adhering to the inside of one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carestream Dental CS 3600 Single Use Normal Tips Recalled by CARESTREAM...
The Issue: The mirror may become detached and fall from the unit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.