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. 1,026 recalls have been distributed to District of Columbia in the last 12 months.
Showing 13081–13100 of 47,654 recalls
Recalled Item: DigitalDiagnost C50 1.1 Recalled by Philips North America Llc Due to...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lum Lam Custom Pack - Anesthesia Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Pack - Surgical Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane- in combination with a Siemens Healthineers table...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: Product is mislabeled as self-righting Luer slip tip caps, yellow.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coryell Memorial Hosp Total Recalled by Stradis Medical, LLC dba Stradis...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S Recalled by...
The Issue: Devices distributed lacked regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno- in combination with a Siemens Healthineers table or Recalled by...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor in combination with a Siemens Healthineers table Recalled...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgicare Neuro Pack - Neurological Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical, Inc. Due to...
The Issue: Lack of sterility assurance: leaking bags
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: hydrALAZINE HCl Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SpaceOAR Vue System Recalled by Boston Scientific Corporation Due to Users...
The Issue: Users need to be aware that embolism is a possible adverse event associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer Packaging Label: Protekt Sharps Safety Knives - 44620MU Recalled by...
The Issue: Surgical knives may contain incorrect description printed on handles....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Custom Procedure Kits containing BD Luer Lok Access Devices Recalled...
The Issue: Recalled devices were packaged in convenience kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceOAR System Recalled by Boston Scientific Corporation Due to Users need...
The Issue: Users need to be aware that embolism is a possible adverse event associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (a) CareFusion Snowden-Pencer Plastics Recalled by Carefusion 2200 Inc Due...
The Issue: The finished device package did not contain the IFU.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to If the...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.