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. 2,656 recalls have been distributed to District of Columbia in the last 12 months.
Showing 881–900 of 47,654 recalls
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: An out of specification results observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Welch Allyn INF BAG Recalled by Baxter Healthcare Corporation Due to...
The Issue: Replacement bladder kit for the Welch Allyn two-piece reusable blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Kits/ containing flow cells Recalled by Illumina, Inc. Due to An...
The Issue: An instrument intended for sequencing DNA libraries with in vitro diagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% SODIUM CHLORIDE Injection Recalled by Otsuka ICU Medical LLC Due to...
The Issue: Lack of Assurance of Sterility: Potential for flexible container leaks.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDLINE PERFUSION SYRINGE Recalled by Medline Industries, LP Due to Medline...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis System Recalled by Nipro Medical Corporation Due to Screw may...
The Issue: Screw may loosen or fallout of Hemodialysis system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iX10...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: elite...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM8...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.