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. 1,056 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3881–3900 of 27,451 recalls
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Blunt Tip Recalled by MEDLINE...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000864 Recalled by ICU Medical Inc Due...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN BACTISEAL EVD Catheter Set - Indicated for gaining access Recalled by...
The Issue: Defect in the external sterile packaging (pouch) leading to a gap or/and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360/A+ spare batteries. Item Number: SUB0000864. Recalled by ICU...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Extremity convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Special Procedure Pack convenience kit Recalled by...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaGuide 2 Intelligent Ultrasound Recalled by NovaSignal Corp. Due to Due...
The Issue: Due to inadvertently disconnecting grounding cable of ultrasound system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Biopsy Drape Pack convenience kit Recalled by...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Spine Pack convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Gyn Laparoscopy convenience kit Recalled by...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Hand Pack convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaGuide 2 Traditional Ultrasound Recalled by NovaSignal Corp. Due to Due...
The Issue: Due to inadvertently disconnecting grounding cable of ultrasound system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Cataract Pack convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Laparoscopy Litho Std Pack convenience kit and...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HA FlexTrak II-Patient transport functionality to transport the patient from...
The Issue: Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.