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. 2,635 recalls have been distributed to District of Columbia in the last 12 months.
Showing 5321–5340 of 47,654 recalls
Recalled Item: ZOLL Powerheart G5 AED Recalled by Zoll Medical Corporation Due to G5...
The Issue: G5 Semi-Automatic AED is shipped, with a protective film over its front...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturesPlus ULTRA T-MALE Maximum Strength Testosterone Boost for Men 60...
The Issue: Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed...
The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturesPlus T-MALE Liquid Testosterone Support for Men 8 OZ Berry Recalled...
The Issue: Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ABL800 FLEX Model Numbers 393-800 and 393-801 The ABL800 FLEX Recalled by...
The Issue: Issue with analyzer when the pH of the calibration solution decreases during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive SuperPulsed Laser System Wireless Footswitch Recalled by Olympus...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC-KEY* Gastric-Jejunal Feeding Tube Kit Recalled by Avanos Medical, Inc....
The Issue: The IFU was missing some risk information requested by another country to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for...
The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MP - Intended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Premium SuperPulsed Laser System Recalled by Olympus Corporation of...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Vertix MD - The Vertix MD Trauma has been Recalled by Siemens Medical...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Complete 30C/200C Homeopathic Kit Recalled by Washington Homeopathic...
The Issue: Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AXIOM MULTIX MP - Inended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Pro SuperPulsed Laser System Recalled by Olympus Corporation of the...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Vertix Solitaire - The Vertix MD Trauma has been Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.