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. 2,655 recalls have been distributed to District of Columbia in the last 12 months.
Showing 2201–2220 of 47,654 recalls
Recalled Item: Kilwin's Family Assortment 9oz Kilwin's Family Recalled by Kilwin's Quality...
The Issue: undeclared pecans
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kilwin's Mocha Truffle bulk 2.5lbs Kilwin's Mocha Truffles 4.75oz Recalled...
The Issue: undeclared pecans
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O-arm O2 Imaging System. Mobile X-Ray System. Recalled by Medtronic...
The Issue: A mechanical component that supports the O2 gantry to the support structure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STICK Recalled by Microbiologics Inc Due to Affected products were...
The Issue: Affected products were packaged with the incorrect KWIK STIK assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barco MNA with the HexaVue IP Integration System Recalled by Steris...
The Issue: This is a sub-recall of event RES 96885. The supplier identified that during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoclopramide Tablets Recalled by Teva Pharmaceuticals USA, Inc Due to...
The Issue: Presence of foreign tablets/capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories, LLC Due to...
The Issue: Failed Impurities/Degradation Specifications An out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories, LLC Due to...
The Issue: Failed Impurities/Degradation Specifications An out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spectrum Advanced Gel Hand Sanitizer Recalled by Consumer Product Partners,...
The Issue: Subpotent product: Product has cloudy appearance and tested below assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to GE HealthCare...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA PET/MR Recalled by GE Medical Systems, LLC Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apex Knee System. Model Numbers: KC-50090 Recalled by CORIN MEDICAL, LTD....
The Issue: Investigation has identified that the age of the nylon packaging material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.