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. 2,591 recalls have been distributed to District of Columbia in the last 12 months.
Showing 11401–11420 of 47,654 recalls
Recalled Item: PrednisoLONE Oral Solution USP Recalled by Akorn, Inc Due to Defective...
The Issue: Defective Container: Product has incomplete induction seals.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Randox Serology I Positive Control contains the following analytes...
The Issue: ***Update** :HBsAg analyte is also Non-Reactive on the Ortho Vitros analyser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 IN (17 cm) APPX 0.78 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroClave Clear Neutral Connector Recalled by ICU Medical, Inc. Due to Due...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" (15 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroClave Clear Neutral Connector. A bidirectional connector used as an...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.5" (22 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx 0.84 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Banana Boat hair & scalp defense Recalled by Edgewell Personal Care Brands,...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kits: Single Pigtail Catalog Number: 6501...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6533) Catalog Number: 6507...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Transbronchial Aspiration Needle Catalog Number: 4621 Recalled by...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4722 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Grasping Forceps Catalog Number:5004 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4565-OLY Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6568) Catalog Number: 6529...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits (contains 3412) Catalog Number: 6027...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.