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. 2,584 recalls have been distributed to District of Columbia in the last 12 months.
Showing 12341–12360 of 47,654 recalls
Recalled Item: Nitrofurantoin Capsules Recalled by American Health Packaging Due to Failed...
The Issue: Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sirolimus Oral Solution Recalled by Apotex Corp. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Keto Living Sugar Control Recalled by Natural Organics, Inc. Due to...
The Issue: Contains undeclared wheat (gluten) in product labeled "gluten free"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: illumina Model NextSeq 550 Dx Recalled by Illumina, Inc. Due to...
The Issue: cybersecurity vulnerability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: illumina Model: MiSeq Dx illumina Model: Recalled by Illumina, Inc. Due to...
The Issue: cybersecurity vulnerability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STORZ KARL STORZ-ENDOSKOPE CMOS Video Cysto-Urethroscope Recalled by Karl...
The Issue: The endoscope may experience a loss of image when activating monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ratcheting Screwdriver Handle Recalled by Tornier, Inc Due to The device is...
The Issue: The device is unable to meet sterilization requirements when sterilized per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MVASI (bevacizumab-awwb) Recalled by Amgen, Inc. Due to Defective container:...
The Issue: Defective container: loose crimp defect, potential loss of container integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablet Recalled by SUN...
The Issue: Presence Of Foreign Substance: Customer complaint for the presence of dark,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablet Recalled by SUN...
The Issue: Presence Of Foreign Substance: Customer complaint for the presence of dark,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adult Cap-ONE Biteblock The cap-ONE Biteblock is intended Recalled by Nihon...
The Issue: Due to products being shipped/distributed to customers after the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM CONTACT EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERGARD Woven Vascular Graft is a woven polyester graft coated Recalled by...
The Issue: Mislabeled: Product labeled as Intergard Woven Straight graft , D: 8 mm, L:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xanax XR (alprazolam) extended-release tablets Recalled by Viatris Inc Due...
The Issue: Failed Dissolution Specifications: low out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: alprazolam XR extended-release tablets Recalled by Viatris Inc Due to Failed...
The Issue: Failed Dissolution Specifications: low out-of-specification dissolution test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Honey Caramels Blue Raspberry. Product available in 5.87 oz. bag Recalled by...
The Issue: Products may potentially contain one or more of the following undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.