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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 25281–25300 of 27,451 recalls
Recalled Item: NovaPACS versions 7.4 Recalled by Novarad Corporation Due to Potential for...
The Issue: Potential for images to be flipped while streaming, which could incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8 mm Monopolar Curved Scissors (a.k.a. Hot Shears) Manufactured and Recalled...
The Issue: Intuitive Surgical has identified a potential for some units of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8mm Maryland Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy LifeLiner Stick & Cut Resistant Gloves Rt Recalled by DePuy...
The Issue: LifeLiner Stick and Cut Resistant Gloves are being recalled because cases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8mm Precise Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Video Laryngoscope (GVL) 3 Recalled by Verathon, Inc. Due to...
The Issue: Verathon GlideScope Reusable GVL and AVL Blades are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8mm Fenestrated Bipolar Forceps used in conjunction with the da Recalled by...
The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Zimmer Air Dermatome Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InSpan Inserter Recalled by SpineFrontier, Inc. Due to Potential for set...
The Issue: Potential for set screw to be come deformed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...
The Issue: This removal is in response to complaints alleging that the Zimmer Air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci 5 mm Flared Instrument Cannulae for use with Recalled by Intuitive...
The Issue: Intuitive Surgical is implementing a voluntary Field Action to implement a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) Chemistry Wash (RD701) Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics received complaints of Chemistry Wash causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System (product code 6802783) Product Usage:...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leucadia Autolok" Polyaxial Pedicle Screw System. Intended to help provide...
The Issue: Alphatec Spine initiated this medical device recall for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System (product code 6802413) Product Usage: For...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro Systems - Luminos dRF Recalled by Siemens Medical...
The Issue: Siemens has discovered through product monitoring a potential malfunction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to There is evidence...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.