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 7541–7560 of 47,654 recalls
Recalled Item: Hysteroscope-For endoscopic diagnosis within the uterus Model Number:...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Water Resistant Pendant with Long Wristband Recalled by Securitas...
The Issue: Premature battery depletion presents a risk that alarms will not be received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Water Resistant Pendant with Wristband Recalled by Securitas...
The Issue: Premature battery depletion presents a risk that alarms will not be received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Water Resistant Pendant with Neck Lanyard Recalled by Securitas...
The Issue: Premature battery depletion presents a risk that alarms will not be received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPRYSTEP VECTOR KAFO Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM SPRYSTEP Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPRYSTEP VECTOR Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of...
The Issue: Units are labeled as 10cc; however the units have a fill volume of 1cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus High-Flow Insufflation Unit Recalled by Olympus Corporation of the...
The Issue: There have been reports of patients suffering arrhythmias, reported as short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2 mcg/mL and bupivacaine 0.125% PF in 0.9% sodium Recalled by...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine in 0.9 sodium chloride Recalled by Central Admixture Pharmacy...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablets USP 10 mg Recalled by Zydus...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine in 0.9 sodium chloride Recalled by Central Admixture Pharmacy...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.