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. 2,438 recalls have been distributed to District of Columbia in the last 12 months.
Showing 33841–33860 of 47,654 recalls
Recalled Item: Germany Niubian Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Herb Viagra Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bigger Longer More Time More Sperms Recalled by R Thomas Marketing, LLC Due...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Super Hard Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: African Black Ant Recalled by R Thomas Marketing, LLC Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bull's Genital Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hard Ten Days Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan...
The Issue: Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Guaifenesin Grape liquid 100 mg/5 mL Recalled by Perrigo Company PLC Due to...
The Issue: Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medix NatalCare ST-LX Intensive Care Incubator. Neonatal incubator. Recalled...
The Issue: NatalCare LX Incubators were manufactured using a defective oval port hinge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kopans Breast Lesion Localization Needle The Kopans Breast Lesion...
The Issue: Product potentially exposed to body fluids during processing. Potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be Recalled by...
The Issue: Increased punch height, causing a 0.063 in (1.6 mm) gap between the trial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus TJF-Q180V flexible gastrointestinal Duodenoscope Product Usage: This...
The Issue: Olympus America Inc is conducting a voluntary removal/corrective action of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0...
The Issue: In DS/US proton planning, there is a correction factor used internally to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API ZYM Bx2 () Product Usage: ZYM B reagent Recalled by BioMerieux SA Due to...
The Issue: Discrepant identification results related to API identification strips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System: HeartWare Battery Recalled by...
The Issue: Heartware Ventricular Assist System Battery Cell experiencing premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Recalled...
The Issue: Some of the Access ClearVue Prone Breast devices may contain scales that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bearded Brothers BOLD Coconut Curry Net Wt. 1.5 oz/43 g . Recalled by...
The Issue: Mold on energy bars.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bearded Brothers BOLD The Greek Net Wt. 1.5 oz/43 g . Recalled by Bearded...
The Issue: Mold on energy bars.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cervical Spine Locking Plate (CSLP) System Recalled by Synthes (USA)...
The Issue: DePuy Synthes is initiating a Voluntary Medical Device Recall of lot #...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.