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. 1,001 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16661–16680 of 47,654 recalls
Recalled Item: DePuy Synthes 15.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 17.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 17.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HVAD Pump Implant Kits Recalled by Heartware, Inc. Due to Pumps...
The Issue: Pumps manufactured with impellers from a subset of lots from a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CM 50-001-01 Injectate Kit Recalled by Lidco Ltd Due to The expiration date...
The Issue: The expiration date on labeling is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The cobas z 480 analyzer including dedicated software for IVD Recalled by...
The Issue: Dirty Lens May Cause Invalid or False Positive Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irinotecan Hydrochloride Injection Recalled by Areva Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: based on a Warning Letter received by the manufacturer of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specifications: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Immune Boost with natural strawberry flavor Recalled by Fusion Health and...
The Issue: Marketed without an Approved NDA/ANDA: Product marketed with drug claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IceFORCE" 2.1 CX Prostate Cryoablation Kit Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinias Recalled by Shimadzu Medical Systems Due to The firm has identified...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IcePearl" 2.1 CX 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bransist Safire Recalled by Shimadzu Medical Systems Due to The firm has...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MH-200S Recalled by Shimadzu Medical Systems Due to The firm has identified...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) Recalled by Becton...
The Issue: BD has confirmed the presence of blood on the cannulas of the BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IcePearl" 2.1 CX L 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed" 1.5 Cryoablation Needle Recalled by Boston Scientific Corporation...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceRod" 1.5 CX 90¿ Cryoablation Needle¿ Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.