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 8121–8140 of 27,451 recalls
Recalled Item: ACS Cath Lab Pack Recalled by American Contract Systems, Inc. Due to Product...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS Lap Chole Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray Recalled by American...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack Recalled by American...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS IR - Angio Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inactivated macrolide-resistant Mycoplasma genitalium Recalled by...
The Issue: The QC process was not adequate for the specification range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restrata Recalled by Acera Surgical Inc Due to Misprinted expiration date on...
The Issue: Misprinted expiration date on the shelf-box
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avanos Cortrak 2 Enteral Access System (EAS) Recalled by Avanos Medical,...
The Issue: Product labeling is being modified. STOP using the Anonymous Account Mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS Recalled by...
The Issue: Ventilator mounting brackets for the Vivo 50/60/65 and Vivo 45LS ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Therapy Management (RTM) VERSIONS 13.6 Recalled by Varian...
The Issue: Software issue for treatment plan and image management application may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic Gastrovideoscope Recalled by Olympus Corporation of the Americas...
The Issue: GF-UC140P-AL5 is no longer a compatible endoscope for reprocessing in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: regard Clinical Packaging...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinici X da Vinci Xi Sureform 45 Recalled by Intuitive Surgical, Inc. Due...
The Issue: As a result of complaint data review, it identified tissue pushout events...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LetsGetChecked Blood Sample Collection kit-In vitro diagnostic medical...
The Issue: Users received sample collection kits that were assigned to another user....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Separation Technology Creamatocrit Plus Recalled by Stanbio Laboratory, LP...
The Issue: The device was being marketed as an IVD without a 510(k). Therefore,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.